Canonical Allele Identifier: PA2826465689
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 844400
ClinVar RCV Id: RCV001047234 RCV001183949 RCV003226427 RCV003467748 RCV004004786
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Glu776Gly
CA346730767
NM_001258281.1:c.2327A>G