Allele Registry

Canonical Allele Identifier: PA2826587469

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000129804

RCV000204360

RCV000409369

RCV000656905

RCV001375525

RCV003467121

RCV004532553

ClinVar Variation:

141327

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Glu1033Ala	CA015298 NM_001281494.2:c.3098A>C