Canonical Allele Identifier: PA645475361
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 265620
ClinVar RCV Id: RCV000255143 RCV000501019 RCV000772137 RCV000803818 RCV001353568
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly692Glu
CA10588345
NM_000251.3:c.2075G>A