Canonical Allele Identifier: PA229281
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102476
ClinVar RCV Id: RCV000088707 RCV001200017
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Tyr343Asp
CA229280
NM_000277.3:c.1027T>G