Allele Registry

Canonical Allele Identifier: PA916012072

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000204738

RCV000566750

RCV000791410

RCV002243889

RCV002277568

RCV003462389

ClinVar Variation:

220745

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Ile898Val	CA071451 NM_001281494.2:c.2692A>G