Canonical Allele Identifier: PA2826942530
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 2768413
ClinVar RCV Id: RCV003517759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001298125.1:p.Glu288Asp
CA351005165
NM_001311196.2:c.864G>C
CA351005166
NM_001311196.2:c.864G>T