Allele Registry

Canonical Allele Identifier: PA2742019253

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV003627211

ClinVar Variation:

2893865

HGVS (amino-acid)	Matching Registered Transcripts
NP_789765.1:p.Thr148Ser	CA378922744 NM_176795.5:c.443C>G CA378922762 NM_176795.5:c.442A>T