Allele Registry

Canonical Allele Identifier: PA2826635148

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000773367

RCV001869094

ClinVar Variation:

628706

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Phe267Ser	CA346748546 NM_001281494.2:c.800T>C