Allele Registry

Canonical Allele Identifier: PA2826631998

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000034496

RCV000115393

RCV000235185

RCV000410628

RCV001080247

RCV003492327

RCV003594839

ClinVar Variation:

41591

2698505

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Gln587His	CA010704 NM_001281493.2:c.1761G>T CA346755231 NM_001281493.2:c.1761G>C