Canonical Allele Identifier: PA2826284115
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2931869
ClinVar RCV Id: RCV003792891

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193471.1:p.Gln258Glu
CA350286855
NM_001206542.2:c.772C>G