Allele Registry

Canonical Allele Identifier: PA2826631358

Gene: MSH6 HGNC NCBI

ClinVar Allele:

226305

ClinVar RCV:

RCV000210157

RCV000215593

RCV001044010

ClinVar Variation:

224581

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Ala435Val	CA357802 NM_001281493.2:c.1304C>T