Canonical Allele Identifier: PA105172
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102846
ClinVar RCV Id: RCV000089105 RCV000153632
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg270Lys
CA229781
NM_000277.3:c.809G>A