Allele Registry

Canonical Allele Identifier: PA2580106099

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002269192

RCV003759091

ClinVar Variation:

1697908

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Thr605Ala	CA068168 NM_000179.3:c.1813A>G