Canonical Allele Identifier: PA2826942184
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 895990
ClinVar RCV Id: RCV001138389 RCV001138388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001298124.1:p.Arg26Lys
CA431952147
NM_001311195.2:c.77G>A