Allele Registry

Canonical Allele Identifier: PA916011415

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000131245

RCV000148653

RCV000212678

RCV000514075

RCV000764429

RCV001079820

RCV001262368

RCV003325179

RCV004537278

ClinVar Variation:

89360

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Pro957Ser	CA012243 NM_001281492.2:c.2869C>T