Allele Registry

Canonical Allele Identifier: PA2826463408

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000213764

RCV000506029

RCV000548278

RCV002243895

RCV003462428

RCV003997816

ClinVar Variation:

230221

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Asn219Lys	CA10577957 NM_001258281.1:c.657C>G CA346732846 NM_001258281.1:c.657C>A