Canonical Allele Identifier: PA2830163911
Gene: ASB10 HGNC NCBI

Linked Data

ClinVar Variation Id: 3130083
ClinVar RCV Id: RCV004420498
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_543147.2:p.Ala162Thr
CA4573859
NM_080871.4:c.484G>A