Canonical Allele Identifier: PA645441134
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 333436
ClinVar RCV Id: RCV000334321
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116759.2:p.Gly439Val
CA10612331
NM_032977.3:c.1316G>T