Canonical Allele Identifier: PA2826401541
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 194006
ClinVar RCV Id: RCV000174260 RCV000530315 RCV001142919 RCV001657944 RCV003891709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243586.1:p.Arg452His
CA200909
NM_001256657.2:c.1355G>A