Canonical Allele Identifier: PA2826283972
Gene: CASP10 HGNC NCBI
ClinVar RCV:
RCV000288669
ClinVar Variation:
333416
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193471.1:p.Lys17Glu
CA2052766
NM_001206542.2:c.49A>G