Canonical Allele Identifier: PA229563
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102688
ClinVar RCV Id: RCV000088936 RCV003479002
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ala156Pro
CA229562
NM_000277.3:c.466G>C