Canonical Allele Identifier: PA645471208
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 232807
ClinVar RCV Id: RCV000222393 RCV000550333 RCV000662879 RCV001762495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met67Lys
CA10577924
NM_000251.3:c.200T>A