Canonical Allele Identifier: PA105144
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 584

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg252Trp
CA057308
NM_000277.3:c.[754C>T;353-507G>T]
CA251529
NM_000277.3:c.754C>T