Canonical Allele Identifier: PA2826465535
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1171756
ClinVar RCV Id: RCV001525120 RCV004008819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn733Ser
CA346730179
NM_001258281.1:c.2198A>G