Allele Registry

Canonical Allele Identifier: PA2825088280

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002397057

ClinVar Variation:

1773483

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu493del	CA2580067595 NM_000179.3:c.1478_1480del