Allele Registry

Canonical Allele Identifier: PA106689

Gene: SIX1 HGNC NCBI

ClinVar RCV:

RCV002477184

ClinVar Variation:

65698

HGVS (amino-acid)	Matching Registered Transcripts
NP_005973.1:p.Val17Glu	CA345039 NM_005982.4:c.50T>A