Allele Registry

Canonical Allele Identifier: PA645474768

Gene: MSH2 HGNC NCBI

ClinVar Variation Id: 246493

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Asn613Tyr	CA10584216 NM_000251.3:c.1837A>T