Allele Registry

Canonical Allele Identifier: PA106631

Gene: SIX1 HGNC NCBI

ClinVar RCV:

RCV000008807

RCV002262561

RCV002512919

ClinVar Variation:

8309

HGVS (amino-acid)	Matching Registered Transcripts
NP_005973.1:p.Arg110Trp	CA340772 NM_005982.4:c.328C>T