Canonical Allele Identifier: PA2826401345
Gene: CHRND HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243586.1:p.Cys136Ser
CA350998285
NM_001256657.2:c.406T>A
CA350998301
NM_001256657.2:c.407G>C