Allele Registry

Canonical Allele Identifier: PA658747685

Gene: MSH6 HGNC NCBI

ClinVar Allele:

483533

2913431

ClinVar RCV:

RCV000582540

RCV001209413

RCV003593730

ClinVar Variation:

491925

2752690

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Val1056Leu	CA46713075 NM_000179.3:c.3166G>C CA346756740 NM_000179.3:c.3166G>T