Canonical Allele Identifier: PA2830108426
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 333416
ClinVar RCV Id: RCV000288669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116756.2:p.Lys17Glu
CA2052766
NM_032974.5:c.49A>G