Allele Registry

Canonical Allele Identifier: PA110707

Gene: PHGDH HGNC NCBI

ClinVar RCV:

RCV000004074

RCV000675113

RCV001171760

ClinVar Variation:

3870

HGVS (amino-acid)	Matching Registered Transcripts
NP_006614.2:p.Arg135Trp	CA116478 NM_006623.4:c.403C>T