Canonical Allele Identifier: PA2580160119
Gene: ASB10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2303098
ClinVar RCV Id: RCV004152661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135932.2:p.Gly171Glu
CA169125197
NM_001142460.1:c.512G>A