Allele Registry

Canonical Allele Identifier: PA915992072

Gene: MSH3 HGNC NCBI

ClinVar RCV:

RCV001018762

RCV001520312

RCV002018971

ClinVar Variation:

822964

1478283

HGVS (amino-acid)	Matching Registered Transcripts
NP_002430.3:p.Ala1045Thr	CA3328468 NM_002439.5:c.3133G>A CA2573139916 NM_002439.5:c.3132_3133delinsTA