Allele Registry

Canonical Allele Identifier: PA891846105

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000700974

RCV003165866

ClinVar Variation:

578073

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Pro462Leu	CA346745042 NM_000179.3:c.1385C>T