Canonical Allele Identifier: PA891863954
Gene: PHGDH HGNC NCBI

Linked Data

ClinVar Variation Id: 591900
ClinVar RCV Id: RCV000723083
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006614.2:p.Thr147Pro
CA341847719
NM_006623.4:c.439A>C