Allele Registry

Canonical Allele Identifier: PA916011330

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000582540

RCV001209413

RCV003593730

ClinVar Variation:

491925

2752690

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Val926Leu	CA46713075 NM_001281492.2:c.2776G>C CA346756740 NM_001281492.2:c.2776G>T