Canonical Allele Identifier: PA2826283874
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1014291
ClinVar RCV Id: RCV001796873
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193453.1:p.Ser362Gly
CA350292522
NM_001206524.2:c.1084A>G