Canonical Allele Identifier: PA2827255467
Gene: PARL HGNC NCBI

Linked Data

ClinVar Variation Id: 3208656
ClinVar RCV Id: RCV004502552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311365.1:p.Arg76Thr
CA2723630
NM_001324436.2:c.227G>C