Allele Registry

Canonical Allele Identifier: PA2826636521

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000160683

RCV000205971

RCV000759138

RCV000781587

RCV001142302

RCV003462094

RCV003998497

ClinVar Variation:

182637

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Lys586Asn	CA010696 NM_001281494.2:c.1758G>C CA346755217 NM_001281494.2:c.1758G>T