Canonical Allele Identifier: PA2830108860
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 21728
ClinVar RCV Id: RCV000020931 RCV001668132
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116756.2:p.Tyr446Cys
CA342419
NM_032974.5:c.1337A>G