Allele Registry

Canonical Allele Identifier: PA658826399

Gene: GCDH HGNC NCBI

ClinVar Allele:

549092

ClinVar RCV:

RCV000665802

ClinVar Variation:

550912

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Ser139Trp	CA404317502 NM_000159.4:c.416C>G