Canonical Allele Identifier: PA2826401483
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 193603
ClinVar RCV Id: RCV000173709 RCV000224550 RCV001079470 RCV001198096 RCV001138073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243586.1:p.Pro354Ser
CA200681
NM_001256657.2:c.1060C>T