Canonical Allele Identifier: PA2826465375
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479790
ClinVar RCV Id: RCV000565456 RCV000759112 RCV000793685 RCV004000849
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Thr690Ala
CA035125
NM_001258281.1:c.2068A>G