Allele Registry

Canonical Allele Identifier: PA2826465134

Gene: MSH2 HGNC NCBI

ClinVar Allele:

96356

ClinVar RCV:

RCV000076383

RCV000492029

RCV000501546

RCV001034643

RCV003452886

ClinVar Variation:

90881

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Pro630Leu	CA019979 NM_001258281.1:c.1889C>T