Canonical Allele Identifier: PA2826942564
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 1302902
ClinVar RCV Id: RCV001756401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001298125.1:p.Asn342Ser
CA351005718
NM_001311196.2:c.1025A>G