Canonical Allele Identifier: PA106177
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102581
ClinVar RCV Id: RCV000088819 RCV000993605
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Lys42Ile
CA229419
NM_000277.3:c.125A>T