Canonical Allele Identifier: PA106066
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 578
ClinVar RCV Id: RCV000000608 RCV000089164
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Leu311Pro
CA251524
NM_000277.3:c.932T>C