Allele Registry

Canonical Allele Identifier: PA2826634025

Gene: MSH6 HGNC NCBI

ClinVar Allele:

405964

ClinVar RCV:

RCV000480936

RCV000574295

RCV001348367

RCV004002305

ClinVar Variation:

419537

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Met1024Thr	CA072409 NM_001281493.2:c.3071T>C