Allele Registry

Canonical Allele Identifier: PA248574

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000001827

RCV000076285

RCV000128908

RCV000202293

RCV000524362

RCV001353543

RCV002407706

ClinVar Variation:

1757

1780064

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Asn596del	CA019297 NM_000251.3:c.1786_1788del CA2580066937 NM_000251.3:c.1785_1787del