Canonical Allele Identifier: PA915984165
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 187103
ClinVar RCV Id: RCV000166792 RCV000546078 RCV000997136 RCV001357296 RCV002053989 RCV002267920 RCV002291583
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu69Val
CA021133
NM_001258281.1:c.205C>G