Canonical Allele Identifier: PA104852
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102812
ClinVar RCV Id: RCV000089067 RCV002259592
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ala246Asp
CA229726
NM_000277.3:c.737C>A