Allele Registry

Canonical Allele Identifier: PA106618

Gene: SIX1 HGNC NCBI

ClinVar RCV:

RCV000482613

RCV003223408

ClinVar Variation:

420132

HGVS (amino-acid)	Matching Registered Transcripts
NP_005973.1:p.Arg110Gln	CA16619881 NM_005982.4:c.329G>A