Canonical Allele Identifier: PA105475
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102514
ClinVar RCV Id: RCV000088746 RCV001199978
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Cys357Gly
CA229329
NM_000277.3:c.1069T>G