Canonical Allele Identifier: PA915984161
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 487004
ClinVar RCV Id: RCV000563996 RCV001324767 RCV004001204
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asp67Gly
CA46677666
NM_001258281.1:c.200A>G