Canonical Allele Identifier: PA645472018
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408527
ClinVar RCV Id: RCV000568397 RCV000467943 RCV001171949 RCV003335335 RCV004000790
ClinVar Variation Id: 2584100
ClinVar RCV Id: RCV003335548
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met253Ile
CA16610795
NM_000251.3:c.759G>A
CA346732367
NM_000251.3:c.759G>C
CA346732369
NM_000251.3:c.759G>T