Allele Registry

Canonical Allele Identifier: PA2826637248

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000582540

RCV001209413

RCV003593730

ClinVar Variation:

491925

2752690

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Val754Leu	CA46713075 NM_001281494.2:c.2260G>C CA346756740 NM_001281494.2:c.2260G>T