Canonical Allele Identifier: PA2826401304
Gene: CHRND HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243586.1:p.Lys74Asn
CA2167978
NM_001256657.2:c.222G>C
CA350997423
NM_001256657.2:c.222G>T