Allele Registry

Canonical Allele Identifier: PA2826464320

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000580795

RCV003452837

ClinVar Variation:

90684

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Leu437Pro	CA018480 NM_001258281.1:c.1310T>C