Canonical Allele Identifier: PA645471361
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 231062
ClinVar RCV Id: RCV000221016 RCV000702606 RCV003469023
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala107Gly
CA10577932
NM_000251.3:c.320C>G