Allele Registry

Canonical Allele Identifier: PA2579931656

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000150834

RCV000150835

ClinVar Variation:

40435

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123914.1:p.Ala59Thr	CA176353 NM_001130442.3:c.175G>A