Canonical Allele Identifier: PA645472137
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237407
ClinVar RCV Id: RCV000231079 RCV001026925 RCV001193895 RCV003128606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn263Lys
CA10582001
NM_000251.3:c.789T>G
CA346732518
NM_000251.3:c.789T>A