Allele Registry

Canonical Allele Identifier: PA109583

Gene: ST14 HGNC NCBI

ClinVar RCV:

RCV000004253

ClinVar Variation:

4038

HGVS (amino-acid)	Matching Registered Transcripts
NP_068813.1:p.Gly827Arg	CA116624 NM_021978.4:c.2479G>A CA230708439 NM_021978.4:c.2479G>C