Canonical Allele Identifier: PA332423
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135854
ClinVar RCV Id: RCV000122982 RCV000235661 RCV000580136 RCV000657006 RCV002477321 RCV003460870 RCV003997405
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu56Lys
CA018954
NM_000251.3:c.166G>A