Canonical Allele Identifier: PA658671630
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455588
ClinVar RCV Id: RCV000524887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn115Tyr
CA346730057
NM_000251.3:c.343A>T