Allele Registry

Canonical Allele Identifier: PA916011344

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000216009

RCV000691203

RCV000759861

RCV003997246

ClinVar Variation:

127581

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ala934Val	CA011826 NM_001281492.2:c.2801C>T