Allele Registry

Canonical Allele Identifier: PA915953478

Gene: MSH2 HGNC NCBI

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Phe519Leu	CA346727792 NM_000251.3:c.1555T>C CA346727797 NM_000251.3:c.1557T>A CA346727798 NM_000251.3:c.1557T>G