Canonical Allele Identifier: PA105996
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102768
ClinVar RCV Id: RCV000089018 RCV000671113
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Leu212Pro
CA229668
NM_000277.3:c.635T>C