Canonical Allele Identifier: PA229289
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102481
ClinVar RCV Id: RCV000088712 RCV001543654
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly344Asp
CA229288
NM_000277.3:c.1031G>A