Canonical Allele Identifier: PA2826281634
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 7764
ClinVar RCV Id: RCV000008205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001221.2:p.Leu242Phe
CA340692
NM_001230.5:c.724C>T