Allele Registry

Canonical Allele Identifier: PA2826632010

Gene: MSH6 HGNC NCBI

ClinVar Allele:

231564

ClinVar RCV:

RCV000215122

RCV000473265

RCV001016279

RCV003998617

ClinVar Variation:

234455

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Ile589Met	CA069419 NM_001281493.2:c.1767C>G