Canonical Allele Identifier: PA2580129643
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 2181412
ClinVar RCV Id: RCV002606134 RCV003143501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000742.1:p.Phe401Leu
CA2168287
NM_000751.2:c.1203C>G
CA351005241
NM_000751.2:c.1201T>C
CA351005246
NM_000751.2:c.1203C>A