Canonical Allele Identifier: PA2499274438
Gene: PHGDH HGNC NCBI

Linked Data

ClinVar Variation Id: 1029062
ClinVar RCV Id: RCV001330263 RCV002546379
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006614.2:p.Arg268Trp
CA1037269
NM_006623.4:c.802C>T