ClinGen Allele Registry
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Canonical Allele Identifier:
PA134723
Gene: RAF1
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.2409220206
Score
-0.0516452388
Score
-0.0780720359
Score
-0.0496673364
Score
-0.1240515493
Score
-0.1201867126
Score
-0.0776471116
Score
-0.0890357055
Score
-0.3152152741
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000037686
RCV000461248
RCV000586687
RCV000620637
RCV004532499
ClinVar Variation:
40588
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_002871.1:p.Asn71Ser
CA134721
NM_002880.4:c.212A>G