Canonical Allele Identifier: PA2826464024
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483719
ClinVar RCV Id: RCV000570734 RCV002528137 RCV004001039
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.His362Asp
CA346724494
NM_001258281.1:c.1084C>G