Allele Registry

Canonical Allele Identifier: PA2826632694

Gene: MSH6 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000132157

RCV000408980

RCV000588824

RCV001030498

RCV001257068

RCV001355067

RCV001796965

RCV003492535

RCV004528840

ClinVar Variation:

135839

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Val749Ile	CA011639 NM_001281493.2:c.2245G>A