Canonical Allele Identifier: PA105237
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102575
ClinVar RCV Id: RCV000088811 RCV001380994
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg413Ser
CA229411
NM_000277.3:c.1237C>A