ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA176354
Gene: HRAS
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.0468443607
Score
0.2189034235
Score
0.0503447777
Score
0.0188073847
Linked Data - NCBI & NCI
ClinVar Allele:
48905
ClinVar RCV:
RCV000150834
RCV000150835
ClinVar Variation:
40435
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_005334.1:p.Ala59Thr
CA176353
NM_005343.4:c.175G>A