Allele Registry

Canonical Allele Identifier: PA2826632717

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000114751

RCV000223291

RCV001216258

RCV003453034

ClinVar Variation:

126892

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Ala753Pro	CA011702 NM_001281493.2:c.2257G>C