Allele Registry

Canonical Allele Identifier: PA2826627996

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000129763

RCV000204094

RCV000410024

RCV002288628

RCV003997522

ClinVar Variation:

141296

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Tyr839Phe	CA011081 NM_001281492.2:c.2516A>T