Allele Registry

Canonical Allele Identifier: PA2826634592

Gene: MSH6 HGNC NCBI

ClinVar Allele:

94660

ClinVar RCV:

RCV000128873

RCV000214282

RCV000791437

RCV002288560

RCV003460660

ClinVar Variation:

89186

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Leu133Pro	CA008468 NM_001281494.2:c.398T>C