Allele Registry

Canonical Allele Identifier: PA915984136

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000030253

RCV000035361

RCV000144619

RCV000162398

RCV000757470

RCV001353586

RCV002490419

RCV003149584

ClinVar Variation:

36577

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Asn61Ser	CA021092 NM_001258281.1:c.182A>G CA3054204375 NM_001258281.1:c.182_186delinsGTCTT