Allele Registry

Canonical Allele Identifier: PA2826463241

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV002380341

ClinVar Variation:

1758545

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Lys180Gln	CA022120 NM_001258281.1:c.538A>C