Canonical Allele Identifier: PA110727
Gene: PHGDH HGNC NCBI

Linked Data

ClinVar Variation Id: 139534
ClinVar RCV Id: RCV000128433 RCV000171157 RCV002514704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006614.2:p.Gly140Arg
CA163241
NM_006623.4:c.418G>A
CA341847673
NM_006623.4:c.418G>C