Canonical Allele Identifier: PA2825311083
Gene: ASB11 HGNC NCBI

Linked Data

ClinVar Variation Id: 782970
ClinVar RCV Id: RCV000964441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001012428.1:p.Arg187Trp
CA10353850
NM_001012428.2:c.559A>T