Canonical Allele Identifier: PA229489
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102631
ClinVar RCV Id: RCV000088874 RCV002259586
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ser70Pro
CA229488
NM_000277.3:c.208T>C