Allele Registry

Canonical Allele Identifier: PA2826462777

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000460763

RCV000523794

RCV000575381

RCV004000791

ClinVar Variation:

408535

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Met17Val	CA16610775 NM_001258281.1:c.49A>G