Allele Registry

Canonical Allele Identifier: PA2573198602

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV001953316

ClinVar Variation:

1443090

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304983.1:p.His16Gln	CA378923304 NM_001318054.2:c.48C>G CA378923309 NM_001318054.2:c.48C>A