Allele Registry

Canonical Allele Identifier: PA916010918

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000164343

RCV000793874

RCV001795287

RCV003462130

ClinVar Variation:

184992

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Pro15Ser	CA015522 NM_001281492.2:c.43C>T