Canonical Allele Identifier: PA2580347799
Gene: PHGDH HGNC NCBI

Linked Data

ClinVar Variation Id: 2227727
ClinVar RCV Id: RCV002678849
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006614.2:p.Lys170Asn
CA341847861
NM_006623.4:c.510G>C
CA341847862
NM_006623.4:c.510G>T