Canonical Allele Identifier: PA1139680065
Gene: CHRND HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000742.1:p.Lys89Asn
CA2167978
NM_000751.2:c.267G>C
CA350997423
NM_000751.2:c.267G>T