Canonical Allele Identifier: PA2826942317
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 2010119
ClinVar RCV Id: RCV002850956
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001298124.1:p.Lys265Glu
CA351005887
NM_001311195.2:c.793A>G