Canonical Allele Identifier: PA2573252263
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1446933
ClinVar RCV Id: RCV001987973

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Gly181Arg
CA10228660
NM_006941.4:c.541G>C
CA324163691
NM_006941.4:c.541G>A