Allele Registry

Canonical Allele Identifier: PA645474790

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000780453

RCV002413352

RCV003449268

ClinVar Variation:

427606

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Pro622Gln	CA346728465 NM_000251.3:c.1865C>A