Canonical Allele Identifier: PA916022177
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 644041
ClinVar RCV Id: RCV000797879 RCV001592979 RCV002501060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Arg82Cys
CA5779222
NM_001318054.2:c.244C>T