Allele Registry

Canonical Allele Identifier: PA2826464734

Gene: MSH2 HGNC NCBI

ClinVar Allele:

518439

ClinVar RCV:

RCV000629723

RCV001013211

RCV001731820

RCV004002772

ClinVar Variation:

525615

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ala538Thr	CA346728336 NM_001258281.1:c.1612G>A