Canonical Allele Identifier: PA2826401487
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 2873829
ClinVar RCV Id: RCV003633204
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243586.1:p.Val360Leu
CA2168269
NM_001256657.2:c.1078G>T
CA351005075
NM_001256657.2:c.1078G>C