Canonical Allele Identifier: PA105946
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102623

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ile65Asn
CA229479
NM_000277.3:c.194T>A