Allele Registry

Canonical Allele Identifier: PA2826463240

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000630037

RCV001026328

ClinVar Variation:

525763

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Lys180Glu	CA346732225 NM_001258281.1:c.538A>G