Allele Registry

Canonical Allele Identifier: PA658801896

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000630129

RCV001024658

RCV002483771

RCV004002791

ClinVar Variation:

525808

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Asp197His	CA46703403 NM_000179.3:c.589G>C