Allele Registry

Canonical Allele Identifier: PA2825092098

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002875937

ClinVar Variation:

2023785

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Lys1233del	CA2580067289 NM_000179.3:c.3697_3699del