Allele Registry

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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