Allele Registry

Canonical Allele Identifier: PA160911

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_000170.1:p.Pro1087His	CA012253 NM_000179.3:c.3260C>A