Canonical Allele Identifier: PA094750
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 427603
ClinVar RCV Id: RCV000490598 RCV000491547 RCV001039917
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asp660Gly
CA346728864
NM_000251.3:c.1979A>G