Canonical Allele Identifier: PA2825137864
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 872776
ClinVar RCV Id: RCV001093427

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ala49Asp
CA386302329
NM_000277.3:c.146C>A