Canonical Allele Identifier: PA915978901
Gene: ASB10 HGNC NCBI

Linked Data

ClinVar Variation Id: 99944

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135932.2:p.Ala75Glu
CA150466
NM_001142460.1:c.224C>A