Allele Registry

Canonical Allele Identifier: PA2826633531

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002348936

ClinVar Variation:

1734109

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Leu933_Glu935del	CA2580067291 NM_001281493.2:c.2796_2804del