Canonical Allele Identifier: PA2825138206
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 932278
ClinVar RCV Id: RCV001200015
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Tyr377Asp
CA16020946
NM_000277.3:c.1129T>G