Canonical Allele Identifier: PA2826283891
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1951627
ClinVar RCV Id: RCV002686305 RCV004066889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193453.1:p.Cys396Ser
CA2053233
NM_001206524.2:c.1186T>A
CA350293270
NM_001206524.2:c.1187G>C