Allele Registry

Canonical Allele Identifier: PA1139723056

Gene: MSH3 HGNC NCBI

ClinVar RCV:

RCV001035801

RCV001224842

RCV002454265

RCV004032521

ClinVar Variation:

835003

952685

HGVS (amino-acid)	Matching Registered Transcripts
NP_002430.3:p.Ile79Leu	CA360265736 NM_002439.5:c.235A>C CA360265738 NM_002439.5:c.235A>T