Canonical Allele Identifier: PA2826284110
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 333431
ClinVar RCV Id: RCV000327608 RCV004021789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193471.1:p.Ser250Arg
CA2053088
NM_001206542.2:c.750C>A
CA350286539
NM_001206542.2:c.748A>C
CA350286558
NM_001206542.2:c.750C>G