Canonical Allele Identifier: PA2826401524
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 2164221
ClinVar RCV Id: RCV003082044
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243586.1:p.Asn418Ser
CA2168320
NM_001256657.2:c.1253A>G