Canonical Allele Identifier: PA916071805
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 618166
ClinVar RCV Id: RCV000756250
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Met72Leu
CA378924601
NM_176795.5:c.214A>T
CA378924603
NM_176795.5:c.214A>C