Canonical Allele Identifier: PA106114
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102573
ClinVar RCV Id: RCV000088809 RCV001093507
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Leu41Pro
CA229408
NM_000277.3:c.122T>C