Canonical Allele Identifier: PA1139676105
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 927599
ClinVar RCV Id: RCV001190993 RCV003770150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala15Val
CA346728545
NM_000251.3:c.44C>T