ClinGen Allele Registry
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Canonical Allele Identifier:
PA2829600822
Gene: HRAS
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.2097888161
Score
-0.0997778248
Score
0.3312663896
Score
0.0024412912
Linked Data - NCBI & NCI
ClinVar Allele:
1325102
ClinVar RCV:
RCV001813657
RCV002541490
ClinVar Variation:
1334242
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_005334.1:p.Ala59Ser
CA378924686
NM_005343.4:c.175G>T