Allele Registry

Canonical Allele Identifier: PA2826464255

Gene: MSH2 HGNC NCBI

ClinVar Allele:

472905

ClinVar RCV:

RCV000573636

RCV001043758

RCV002497215

RCV004001118

ClinVar Variation:

485836

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Met419Thr	CA346726967 NM_001258281.1:c.1256T>C