Canonical Allele Identifier: PA150471
Gene: ASB10 HGNC NCBI

Linked Data

ClinVar Variation Id: 99946
ClinVar RCV Id: RCV000086396 RCV002513929
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_543147.2:p.Val334Ala
CA150470
NM_080871.4:c.1001T>C