Canonical Allele Identifier: PA916037358
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102569
ClinVar RCV Id: RCV000088803 RCV000697659
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Leu41Phe
CA229401
NM_001354304.2:c.121C>T