Canonical Allele Identifier: PA1139717263
Gene: PHGDH HGNC NCBI

Linked Data

ClinVar Variation Id: 990734
ClinVar RCV Id: RCV001278818

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006614.2:p.Met169Leu
CA1037117
NM_006623.4:c.505A>T
CA341847848
NM_006623.4:c.505A>C