Canonical Allele Identifier: PA916021164
Gene: CHRND HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001298125.1:p.Cys50Ser
CA350998285
NM_001311196.2:c.148T>A
CA350998301
NM_001311196.2:c.149G>C