Allele Registry

Canonical Allele Identifier: PA916010009

Gene: SIX1 HGNC NCBI

ClinVar RCV:

RCV000825046

RCV000857227

RCV001799516

ClinVar Variation:

666609

HGVS (amino-acid)	Matching Registered Transcripts
NP_005973.1:p.Tyr129Ser	CA389910423 NM_005982.4:c.386A>C