Canonical Allele Identifier: PA331448
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90874
ClinVar RCV Id: RCV000076376 RCV000491088 RCV000524375 RCV001284172 RCV001353848 RCV001804825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met688Arg
CA019937
NM_000251.3:c.2063T>G