Canonical Allele Identifier: PA2825251912
Gene: CHRND HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000742.1:p.Cys151Ser
CA350998285
NM_000751.2:c.451T>A
CA350998301
NM_000751.2:c.452G>C