Allele Registry

Canonical Allele Identifier: PA1139699165

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV001232757

RCV004033178

ClinVar Variation:

959406

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304983.1:p.Pro34Ser	CA378922896 NM_001318054.2:c.100C>T