Allele Registry

Canonical Allele Identifier: PA2580347795

Gene: PHGDH HGNC NCBI

ClinVar RCV:

RCV002904904

ClinVar Variation:

2051719

HGVS (amino-acid)	Matching Registered Transcripts
NP_006614.2:p.Arg135Gly	CA1037075 NM_006623.4:c.403C>G