Canonical Allele Identifier: PA150497
Gene: ASB10 HGNC NCBI

Linked Data

ClinVar Variation Id: 99959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_543147.2:p.Arg174Trp
CA150496
NM_080871.4:c.520C>T