Allele Registry

Canonical Allele Identifier: PA2826464382

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000235347

RCV000566599

ClinVar Variation:

246000

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Tyr455Phe	CA10584215 NM_001258281.1:c.1364A>T