Allele Registry

Canonical Allele Identifier: PA2826636173

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000564287

RCV000815080

RCV000985832

RCV004000878

ClinVar Variation:

479914

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Ile503Val	CA46711082 NM_001281494.2:c.1507A>G