Canonical Allele Identifier: PA2826463043
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 220812
ClinVar RCV Id: RCV000204459 RCV000480096 RCV000772140 RCV003997653
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys131Glu
CA348678
NM_001258281.1:c.391A>G