Canonical Allele Identifier: PA2580337894
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1704713
ClinVar RCV Id: RCV002283040
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Pro303Ser
CA10228570
NM_006941.4:c.907C>T
CA2580099761
NM_006941.4:c.906_907delinsTT