Canonical Allele Identifier: PA2573250381
Gene: PHGDH HGNC NCBI

Linked Data

ClinVar Variation Id: 1449601
ClinVar RCV Id: RCV002014551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006614.2:p.Asp274Glu
CA1037274
NM_006623.4:c.822C>A
CA341851131
NM_006623.4:c.822C>G