Canonical Allele Identifier: PA915978913
Gene: ASB10 HGNC NCBI

Linked Data

ClinVar Variation Id: 727784
ClinVar RCV Id: RCV000902176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135932.2:p.Val131Ala
CA4573899
NM_001142460.1:c.392T>C