Canonical Allele Identifier: PA229390
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102561
ClinVar RCV Id: RCV000672156 RCV000088795
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg400Lys
CA229389
NM_000277.3:c.1199G>A