Allele Registry

Canonical Allele Identifier: PA915984025

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000115526

RCV000475276

RCV000567258

RCV001269195

RCV003467047

RCV003997277

ClinVar Variation:

127642

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Lys44Gln	CA021018 NM_001258281.1:c.130A>C