Canonical Allele Identifier: PA916071732
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 561731
ClinVar RCV Id: RCV000681108 RCV001861890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Ile46Thr
CA378924769
NM_176795.5:c.137T>C