Canonical Allele Identifier: PA357778
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 224575
ClinVar RCV Id: RCV000210074 RCV000568248 RCV000629900 RCV000482758 RCV002267950 RCV003468974
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln397His
CA357776
NM_000251.3:c.1191A>T
CA346733889
NM_000251.3:c.1191A>C