Canonical Allele Identifier: PA2827255498
Gene: PARL HGNC NCBI

Linked Data

ClinVar Variation Id: 3208657
ClinVar RCV Id: RCV004502553

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311367.1:p.Ser97Asn
CA2723618
NM_001324438.2:c.290G>A