Allele Registry

Canonical Allele Identifier: PA2826587471

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000168100

RCV000213342

RCV000663216

RCV001800508

RCV003462256

RCV003987391

RCV003995607

ClinVar Variation:

188188

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Glu1033Asp	CA015307 NM_001281494.2:c.3099A>C CA346761626 NM_001281494.2:c.3099A>T