Allele Registry

Canonical Allele Identifier: PA168638

Gene: MSH6 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

94950

ClinVar RCV:

RCV000131709

RCV000454725

RCV000662523

RCV000759868

RCV001082428

RCV001357732

RCV003448259

RCV003492403

ClinVar Variation:

89476

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Thr1284Met	CA014580 NM_000179.3:c.3851C>T