Canonical Allele Identifier: PA2826401507
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 2100002
ClinVar RCV Id: RCV003014194

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243586.1:p.Glu391Asp
CA351005280
NM_001256657.2:c.1173G>C
CA351005281
NM_001256657.2:c.1173G>T