Canonical Allele Identifier: PA916037655
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102860
ClinVar RCV Id: RCV000089121 RCV000411640
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Tyr277Cys
CA229800
NM_001354304.2:c.830A>G