Canonical Allele Identifier: PA1139690654
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 140785
ClinVar RCV Id: RCV000128935 RCV000168369 RCV000202257 RCV000410609 RCV000656885 RCV000664314
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Glu793_Gln795del
CA020756
NM_001258281.1:c.2378_2386del