Canonical Allele Identifier: PA105101
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102803
ClinVar RCV Id: RCV000089054 RCV000153635
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg241Cys
CA273357
NM_000277.3:c.721C>T