Allele Registry

Canonical Allele Identifier: PA117664

Gene: CST3 HGNC NCBI

ClinVar RCV:

RCV000005989

RCV001777132

RCV002054421

RCV002490325

ClinVar Variation:

5635

HGVS (amino-acid)	Matching Registered Transcripts
NP_000090.1:p.Ala25Thr	CA117663 NM_000099.4:c.73G>A