Allele Registry

Canonical Allele Identifier: PA658802017

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000622394

RCV003278952

RCV003451475

RCV003594011

ClinVar Variation:

520541

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.His367Arg	CA346741910 NM_000179.3:c.1100A>G