Canonical Allele Identifier: PA2825251904
Gene: CHRND HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000742.1:p.Trp141Cys
CA350998097
NM_000751.2:c.423G>C
CA350998098
NM_000751.2:c.423G>T