Canonical Allele Identifier: PA2825845961
Gene: ASB10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2303098
ClinVar RCV Id: RCV004152661

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135931.2:p.Gly171Glu
CA169125197
NM_001142459.2:c.512G>A