Allele Registry

Canonical Allele Identifier: PA645378622

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000215713

RCV000555550

RCV000663154

RCV002280111

RCV003462459

RCV003997891

RCV004526646

ClinVar Variation:

231285

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Thr213Pro	CA10578041 NM_000179.3:c.637A>C