Allele Registry

Canonical Allele Identifier: PA357520

Gene: MSH6 HGNC NCBI

ClinVar Allele:

221278

ClinVar RCV:

RCV001012760

RCV001360388

RCV003997648

ClinVar Variation:

220633

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ile570Val	CA068049 NM_000179.3:c.1708A>G