Canonical Allele Identifier: PA2573250325
Gene: PHGDH HGNC NCBI

Linked Data

ClinVar Variation Id: 1488640
ClinVar RCV Id: RCV001980241
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006614.2:p.Trp133Cys
CA341847620
NM_006623.4:c.399G>C
CA341847621
NM_006623.4:c.399G>T