Canonical Allele Identifier: PA2826283858
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 7769
ClinVar RCV Id: RCV000008211
ClinVar Variation Id: 333435
ClinVar RCV Id: RCV000440171 RCV000378446 RCV001258256
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193453.1:p.Ile339Leu
CA340695
NM_001206524.2:c.1015A>C
CA2053200
NM_001206524.2:c.1015A>T