Canonical Allele Identifier: PA1139748281
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 935657
ClinVar RCV Id: RCV001204299
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Lys88Arg
CA378924406
NM_176795.5:c.263A>G