Allele Registry

Canonical Allele Identifier: PA215576

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000034496

RCV000115393

RCV000235185

RCV000410628

RCV001080247

RCV003492327

RCV003594839

ClinVar Variation:

41591

2698505

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gln889His	CA010704 NM_000179.3:c.2667G>T CA346755231 NM_000179.3:c.2667G>C