Canonical Allele Identifier: PA1139717374
Gene: PHGDH HGNC NCBI

Linked Data

ClinVar Variation Id: 874455
ClinVar RCV Id: RCV001097408 RCV001531010 RCV003339478 RCV004032023
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006614.2:p.Arg270Gln
CA1037273
NM_006623.4:c.809G>A