Canonical Allele Identifier: PA645474333
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237367
ClinVar RCV Id: RCV000225970 RCV000573569 RCV000985795 RCV003150132 RCV003338475 RCV003998755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met460Val
CA028135
NM_000251.3:c.1378A>G