Allele Registry

Canonical Allele Identifier: PA110757

Gene: PHGDH HGNC NCBI

ClinVar RCV:

RCV000004072

RCV001262594

ClinVar Variation:

3868

HGVS (amino-acid)	Matching Registered Transcripts
NP_006614.2:p.Val425Met	CA116476 NM_006623.4:c.1273G>A