Allele Registry

Canonical Allele Identifier: PA2826465201

Gene: MSH2 HGNC NCBI

ClinVar Allele:

518447

ClinVar RCV:

RCV000629968

RCV000777516

ClinVar Variation:

525729

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Arg645Leu	CA346729289 NM_001258281.1:c.1934G>T