Allele Registry

Canonical Allele Identifier: PA2826627616

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000484043

RCV000553546

RCV001016203

RCV004003343

ClinVar Variation:

421056

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Lys753Thr	CA069399 NM_001281492.2:c.2258A>C