Allele Registry

Canonical Allele Identifier: PA645471208

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000222393

RCV000550333

RCV000662879

RCV001762495

ClinVar Variation:

232807

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Met67Lys	CA10577924 NM_000251.3:c.200T>A