Canonical Allele Identifier: PA916037612
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_001341233.1:p.Ala259Val
CA229756
NM_001354304.2:c.776C>T