Canonical Allele Identifier: PA1139758248
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 849666
ClinVar RCV Id: RCV001796842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116759.2:p.Ser266Phe
CA2053048
NM_032977.3:c.797C>T