Allele Registry

Canonical Allele Identifier: PA2826637283

Gene: MSH6 HGNC NCBI

ClinVar Allele:

133038

ClinVar RCV:

RCV000216009

RCV000691203

RCV000759861

RCV003997246

ClinVar Variation:

127581

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Ala762Val	CA011826 NM_001281494.2:c.2285C>T