Allele Registry

Canonical Allele Identifier: PA2741940457

Gene: GCDH HGNC NCBI

ClinVar Allele:

3062687

ClinVar RCV:

RCV003603772

ClinVar Variation:

2907540

HGVS (amino-acid)	Matching Registered Transcripts
NP_039663.1:p.Gly354Cys	CA404320276 NM_013976.3:c.1060G>T