Allele Registry

Canonical Allele Identifier: PA106664

Gene: SIX1 HGNC NCBI

ClinVar RCV:

RCV000008809

ClinVar Variation:

8311

HGVS (amino-acid)	Matching Registered Transcripts
NP_005973.1:p.Trp122Arg	CA254384 NM_005982.4:c.364T>A CA389910477 NM_005982.4:c.364T>C