Allele Registry

Canonical Allele Identifier: PA1139676216

Gene: MSH2 HGNC NCBI

ClinVar Allele:

942954

ClinVar RCV:

RCV001230131

RCV002429983

ClinVar Variation:

957192

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Glu28Lys	CA040832 NM_000251.3:c.82G>A