Canonical Allele Identifier: PA645472011
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230783
ClinVar RCV Id: RCV000213414 RCV001853524
ClinVar Variation Id: 861888
ClinVar RCV Id: RCV001068501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln252His
CA040292
NM_000251.3:c.756G>C
CA346732351
NM_000251.3:c.756G>T