Canonical Allele Identifier: PA106832
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102811
ClinVar RCV Id: RCV000089064 RCV000632879
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Val245Glu
CA229725
NM_000277.3:c.734T>A