Canonical Allele Identifier: PA2826462723
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 631150
ClinVar RCV Id: RCV000777305
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly2_Pro3del
CA913187925
NM_001258281.1:c.5_10del