Allele Registry

Canonical Allele Identifier: PA2826463381

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000122993

RCV000131260

RCV000237042

RCV000409770

RCV000656875

RCV003997410

ClinVar Variation:

135865

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Leu213Val	CA022395 NM_001258281.1:c.637C>G