Canonical Allele Identifier: PA2825137851
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1402572
ClinVar RCV Id: RCV001896984
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Glu21Asp
CA6749050
NM_000277.3:c.63A>C
CA386302823
NM_000277.3:c.63A>T