Canonical Allele Identifier: PA2826977561
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 836160
ClinVar RCV Id: RCV001037216 RCV001261055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Ser104Asn
CA378920937
NM_001318054.2:c.311G>A