Allele Registry

Canonical Allele Identifier: PA2826632318

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000561841

RCV000629885

RCV001355686

RCV001374579

RCV001764641

RCV004000884

ClinVar Variation:

479947

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Ile660Thr	CA069760 NM_001281493.2:c.1979T>C