Allele Registry

Canonical Allele Identifier: PA2826629584

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000466844

RCV000579969

RCV004022782

ClinVar Variation:

410445

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Thr21Ile	CA073667 NM_001281493.2:c.62C>T