Allele Registry

Canonical Allele Identifier: PA160897

Gene: MSH6 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000030259

RCV000034490

RCV000121576

RCV000144628

RCV000157762

RCV000625241

RCV001083342

RCV001353801

RCV001798021

ClinVar Variation:

36582

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Leu396Val	CA008249 NM_000179.3:c.1186C>G