Allele Registry

Canonical Allele Identifier: PA331670

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV002380341

ClinVar Variation:

1758545

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Lys246Gln	CA022120 NM_000251.3:c.736A>C