Canonical Allele Identifier: PA106198
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2137411
ClinVar RCV Id: RCV003062537
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Phe121Leu
CA16020777
NM_000277.3:c.361T>C
CA386302255
NM_000277.3:c.363C>G
CA386302256
NM_000277.3:c.363C>A