Allele Registry

Canonical Allele Identifier: PA2825088836

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002413014

ClinVar Variation:

1781327

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gln618_Leu621del	CA2580067715 NM_000179.3:c.1851_1862del