Allele Registry

Canonical Allele Identifier: PA331308

Gene: MSH2 HGNC NCBI

MaveDb:

Score 3.7224942267

ClinVar Allele:

96159

ClinVar RCV:

RCV000580795

RCV003452837

ClinVar Variation:

90684

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Leu503Pro	CA018480 NM_000251.3:c.1508T>C