Canonical Allele Identifier: PA913194998
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 619154
ClinVar RCV Id: RCV000758107 RCV003235382
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asp59Val
CA16020736
NM_000277.3:c.176A>T