Allele Registry

Canonical Allele Identifier: PA274820

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000160681

RCV000172814

RCV000412250

RCV000588994

RCV001084037

RCV003149835

RCV003493450

ClinVar Variation:

135835

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ile795Thr	CA010164 NM_000179.3:c.2384T>C