Canonical Allele Identifier: PA915978890
Gene: ASB10 HGNC NCBI

Linked Data

ClinVar Variation Id: 99991
ClinVar RCV Id: RCV000086441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135932.2:p.Gly65Glu
CA228061
NM_001142460.1:c.194G>A