Allele Registry

Canonical Allele Identifier: PA103722

Gene: HMGCS2 HGNC NCBI

ClinVar RCV:

RCV000009843

ClinVar Variation:

9261

HGVS (amino-acid)	Matching Registered Transcripts
NP_005509.1:p.Val54Met	CA120262 NM_005518.4:c.160G>A