Canonical Allele Identifier: PA2826401337
Gene: CHRND HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243586.1:p.Trp126Cys
CA350998097
NM_001256657.2:c.378G>C
CA350998098
NM_001256657.2:c.378G>T