Canonical Allele Identifier: PA2579921711
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2002625
ClinVar RCV Id: RCV002824738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys773Met
CA346729894
NM_000251.3:c.2318A>T