Allele Registry

Canonical Allele Identifier: PA915984221

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000115532

RCV000148628

RCV000212585

RCV000588226

RCV000662480

RCV000764421

RCV001085983

RCV001262752

RCV001358588

RCV001798267

RCV004528278

ClinVar Variation:

91097

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ile79Met	CA021158 NM_001258281.1:c.237T>G