Allele Registry

Canonical Allele Identifier: PA1139690527

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001045055

ClinVar Variation:

842611

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gln64Glu	CA346730363 NM_001258281.1:c.190C>G