Allele Registry

Canonical Allele Identifier: PA106681

Gene: SIX1 HGNC NCBI

ClinVar RCV:

RCV002477182

ClinVar Variation:

65696

HGVS (amino-acid)	Matching Registered Transcripts
NP_005973.1:p.Val106Gly	CA345037 NM_005982.4:c.317T>G