Canonical Allele Identifier: PA2580347812
Gene: PHGDH HGNC NCBI

Linked Data

ClinVar Variation Id: 2189557
ClinVar RCV Id: RCV002607451
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006614.2:p.Arg268Gln
CA341851092
NM_006623.4:c.803G>A