Canonical Allele Identifier: PA2827255482
Gene: PARL HGNC NCBI

Linked Data

ClinVar Variation Id: 218097
ClinVar RCV Id: RCV000202343

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311366.1:p.Ser77Asn
CA248581
NM_001324437.2:c.230G>A