Canonical Allele Identifier: PA105608
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102634
ClinVar RCV Id: RCV000088877 RCV001389298
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Glu76Ala
CA229492
NM_000277.3:c.227A>C