Canonical Allele Identifier: PA916037823
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 92731
ClinVar RCV Id: RCV000078506 RCV000150075 RCV000622360 RCV003915048
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ala403Val
CA273106
NM_001354304.2:c.1208C>T