Canonical Allele Identifier: PA2825381328
Gene: PARL HGNC NCBI

Linked Data

ClinVar Variation Id: 218097
ClinVar RCV Id: RCV000202343

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001032728.1:p.Ser77Asn
CA248581
NM_001037639.1:c.230G>A