Allele Registry

Canonical Allele Identifier: PA2826633527

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002875937

ClinVar Variation:

2023785

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Lys931del	CA2580067289 NM_001281493.2:c.2791_2793del