Canonical Allele Identifier: PA104915
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 92753
ClinVar RCV Id: RCV000078538 RCV000150082
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ala309Val
CA220592
NM_000277.3:c.926C>T