Canonical Allele Identifier: PA916073855
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 643723

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116759.2:p.Ala441Thr
CA2053221
NM_032977.3:c.1321G>A