Allele Registry

Canonical Allele Identifier: PA2580414317

Gene: SIX2 HGNC NCBI

ClinVar RCV:

RCV002627472

RCV004066663

ClinVar Variation:

1936717

HGVS (amino-acid)	Matching Registered Transcripts
NP_058628.3:p.Gly261Ser	CA346801024 NM_016932.5:c.781G>A