Canonical Allele Identifier: PA2826401534
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 2440044
ClinVar RCV Id: RCV003144944

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243586.1:p.Asn441Tyr
CA351005854
NM_001256657.2:c.1321A>T