Canonical Allele Identifier: PA2825845972
Gene: ASB10 HGNC NCBI

Linked Data

ClinVar Variation Id: 99959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135931.2:p.Arg189Trp
CA150496
NM_001142459.2:c.565C>T