Canonical Allele Identifier: PA2499234122
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 1298858
ClinVar RCV Id: RCV001727188 RCV002032691
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000742.1:p.Met400Ile
CA351005237
NM_000751.2:c.1200G>A
CA351005238
NM_000751.2:c.1200G>C
CA351005239
NM_000751.2:c.1200G>T