Canonical Allele Identifier: PA645420379
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 285364
ClinVar RCV Id: RCV000301874

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ala404Pro
CA10605090
NM_000277.3:c.1210G>C