Allele Registry

Canonical Allele Identifier: PA2826631852

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000276074

RCV000630372

RCV001372750

RCV002256216

RCV003463784

ClinVar Variation:

237160

336443

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Lys552Asn	CA069186 NM_001281493.2:c.1656G>T CA10582064 NM_001281493.2:c.1656G>C