Canonical Allele Identifier: PA2826283975
Gene: CASP10 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193471.1:p.Arg21Cys
CA2052768
NM_001206542.2:c.61C>T