Canonical Allele Identifier: PA2580160120
Gene: ASB10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2373381
ClinVar RCV Id: RCV004210395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135932.2:p.Ala172Thr
CA370035888
NM_001142460.1:c.514G>A