Allele Registry

Canonical Allele Identifier: PA645382438

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000484043

RCV000553546

RCV001016203

RCV004003343

ClinVar Variation:

421056

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Lys883Thr	CA069399 NM_000179.3:c.2648A>C