Allele Registry

Canonical Allele Identifier: PA2826632864

Gene: MSH6 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

133041

ClinVar RCV:

RCV000115410

RCV000121584

RCV000168382

RCV000589544

RCV001787917

RCV001808341

RCV003997248

RCV004528800

ClinVar Variation:

127584

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Pro785His	CA012253 NM_001281493.2:c.2354C>A