Canonical Allele Identifier: PA229362
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102537
ClinVar RCV Id: RCV000088770 RCV001239036
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Tyr386Asp
CA229361
NM_000277.3:c.1156T>G