Allele Registry

Canonical Allele Identifier: PA151472

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000115440

RCV000121575

RCV000588752

RCV000659887

RCV001083709

RCV001180419

RCV001353587

RCV001564013

RCV001798257

RCV002560801

RCV003492405

ClinVar Variation:

89552

921162

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu221Asp	CA016186 NM_000179.3:c.663A>C CA346739374 NM_000179.3:c.663A>T