Allele Registry

Canonical Allele Identifier: PA2826465773

Gene: MSH2 HGNC NCBI

ClinVar Allele:

616657

ClinVar RCV:

RCV000774957

ClinVar Variation:

630048

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gln795Glu	CA346730999 NM_001258281.1:c.2383C>G