Allele Registry

Canonical Allele Identifier: PA645471925

Gene: MSH2 HGNC NCBI

MaveDb:

Score -4.9322783119

ClinVar RCV:

RCV000457050

RCV000519119

RCV000775712

RCV002842857

ClinVar Variation:

408519

2010015

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Asn242Lys	CA16611006 NM_000251.3:c.726C>G CA346732169 NM_000251.3:c.726C>A