Canonical Allele Identifier: PA229770
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102839
ClinVar RCV Id: RCV000089098 RCV000758126
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gln267Glu
CA229769
NM_000277.3:c.799C>G