Canonical Allele Identifier: PA104874
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 602
ClinVar RCV Id: RCV000000633 RCV000089089
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ala259Val
CA229756
NM_000277.3:c.776C>T