Allele Registry

Canonical Allele Identifier: PA645382523

Gene: MSH6 HGNC NCBI

ClinVar Allele:

231564

ClinVar RCV:

RCV000215122

RCV000473265

RCV001016279

RCV003998617

ClinVar Variation:

234455

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ile891Met	CA069419 NM_000179.3:c.2673C>G