Allele Registry

Canonical Allele Identifier: PA2826635739

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000227011

RCV000483631

RCV000580465

RCV000662419

RCV003469132

RCV003998715

ClinVar Variation:

237151

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Met401Val	CA068470 NM_001281494.2:c.1201A>G