Canonical Allele Identifier: PA110707
Gene: PHGDH HGNC NCBI

Linked Data

ClinVar Variation Id: 3870
ClinVar RCV Id: RCV000004074 RCV000675113 RCV001171760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006614.2:p.Arg135Trp
CA116478
NM_006623.4:c.403C>T