Canonical Allele Identifier: PA150523
Gene: ASB10 HGNC NCBI

Linked Data

ClinVar Variation Id: 99972
ClinVar RCV Id: RCV000086422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135931.2:p.Val67Met
CA150522
NM_001142459.2:c.199G>A