Allele Registry

Canonical Allele Identifier: PA2826632399

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000499422

RCV000573654

RCV001350778

RCV002020639

RCV002441213

RCV003470622

ClinVar Variation:

433918

1511890

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Glu681Asp	CA069854 NM_001281493.2:c.2043G>C CA346756238 NM_001281493.2:c.2043G>T