Canonical Allele Identifier: PA106125
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102585
ClinVar RCV Id: RCV000088824 RCV001789756
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Leu430Pro
CA229426
NM_000277.3:c.1289T>C