Canonical Allele Identifier: PA2573206093
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1465203
ClinVar RCV Id: RCV001979309

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ala156Val
CA242485507
NM_001354304.2:c.467C>T