Canonical Allele Identifier: PA658828622
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 548638
ClinVar RCV Id: RCV000662269 RCV002530595
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Glu49Lys
CA378924752
NM_176795.5:c.145G>A