Allele Registry

Canonical Allele Identifier: PA2826463819

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000160581

RCV000203771

RCV000215764

RCV000780458

ClinVar Variation:

182557

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Leu314Ser	CA017337 NM_001258281.1:c.941T>C