Canonical Allele Identifier: PA2741867138
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2691864
ClinVar RCV Id: RCV003494061

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ala259Gly
CA386295500
NM_001354304.2:c.776C>G