Canonical Allele Identifier: PA645472896
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237418
ClinVar RCV Id: RCV000233408
ClinVar Variation Id: 491854
ClinVar RCV Id: RCV000581531 RCV000813559 RCV003736829 RCV004002340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr321Ser
CA10582006
NM_000251.3:c.961A>T
CA346733064
NM_000251.3:c.962C>G