Allele Registry

Canonical Allele Identifier: PA2826463042

Gene: MSH2 HGNC NCBI

ClinVar Allele:

392692

ClinVar RCV:

RCV000458204

RCV000566582

RCV000780450

RCV004000796

RCV004022695

ClinVar Variation:

408556

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Lys131Gln	CA039407 NM_001258281.1:c.391A>C