Canonical Allele Identifier: PA1139748312
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 940277
ClinVar RCV Id: RCV001209828
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Asp92Asn
CA378924350
NM_176795.5:c.274G>A