Canonical Allele Identifier: PA2826942291
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 1008543
ClinVar RCV Id: RCV001305897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001298124.1:p.Arg213Trp
CA2168291
NM_001311195.2:c.637C>T