Canonical Allele Identifier: PA891863955
Gene: PHGDH HGNC NCBI

Linked Data

ClinVar Variation Id: 591203
ClinVar RCV Id: RCV000722380
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006614.2:p.Met169Val
CA341847849
NM_006623.4:c.505A>G