Allele Registry

Canonical Allele Identifier: PA2826464614

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000484349

RCV000581019

RCV000630236

RCV004003366

ClinVar Variation:

421910

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ile511Val	CA030657 NM_001258281.1:c.1531A>G