Allele Registry

Canonical Allele Identifier: PA2579915364

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV002335486

ClinVar Variation:

1742736

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gln395Lys	CA346733843 NM_000251.3:c.1183C>A