Allele Registry

Canonical Allele Identifier: PA916009026

Gene: GCDH HGNC NCBI

ClinVar Allele:

468496

ClinVar RCV:

RCV000531618

RCV004526700

ClinVar Variation:

459951

HGVS (amino-acid)	Matching Registered Transcripts
NP_039663.1:p.Val133Met	CA404317460 NM_013976.3:c.397G>A