Allele Registry

Canonical Allele Identifier: PA645382748

Gene: MSH6 HGNC NCBI

ClinVar Allele:

393088

ClinVar RCV:

RCV000460470

RCV002255396

RCV003470465

ClinVar Variation:

410467

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu919Asp	CA16611013 NM_000179.3:c.2757A>C CA346755433 NM_000179.3:c.2757A>T