Canonical Allele Identifier: PA229852
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102896
ClinVar RCV Id: RCV000089159 RCV003474693
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Leu308Phe
CA229851
NM_000277.3:c.922C>T