Canonical Allele Identifier: PA095655
Gene: PRKN HGNC NCBI

Linked Data

ClinVar Variation Id: 7050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004553.2:p.Arg275Trp
CA254086
NM_004562.3:c.823C>T