Allele Registry

Canonical Allele Identifier: PA2826464935

Gene: MSH2 HGNC NCBI

ClinVar Allele:

96298

ClinVar RCV:

RCV000076325

ClinVar Variation:

90823

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Pro586His	CA019605 NM_001258281.1:c.1757C>A