Canonical Allele Identifier: PA658671347
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455519
ClinVar RCV Id: RCV000538201 RCV000759824 RCV000562322 RCV004003738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys6Glu
CA030563
NM_000251.3:c.16A>G