Canonical Allele Identifier: PA106342
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 621
ClinVar RCV Id: RCV000000652 RCV000089061
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Pro244Leu
CA229721
NM_000277.3:c.731C>T