Canonical Allele Identifier: PA2826401528
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 1302902
ClinVar RCV Id: RCV001756401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243586.1:p.Asn428Ser
CA351005718
NM_001256657.2:c.1283A>G