Canonical Allele Identifier: PA915978960
Gene: ASB10 HGNC NCBI

Linked Data

ClinVar Variation Id: 99946

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135932.2:p.Val349Ala
CA150470
NM_001142460.1:c.1046T>C