Canonical Allele Identifier: PA106448
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102689
ClinVar RCV Id: RCV000088937 RCV000993613
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ser16Pro
CA229564
NM_000277.3:c.46T>C