Canonical Allele Identifier: PA2741867155
Gene: PAH HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Leu321Ile
CA386291549
NM_001354304.2:c.961C>A