Canonical Allele Identifier: PA2825845969
Gene: ASB10 HGNC NCBI

Linked Data

ClinVar Variation Id: 3130084
ClinVar RCV Id: RCV004420499
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135931.2:p.Lys182Asn
CA370035757
NM_001142459.2:c.546A>T
CA370035758
NM_001142459.2:c.546A>C