Allele Registry

Canonical Allele Identifier: PA2826463971

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000473948

RCV000774562

RCV000780437

RCV004000786

ClinVar Variation:

408511

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Pro349Ser	CA16610806 NM_001258281.1:c.1045C>T