Canonical Allele Identifier: PA2579920040
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1714159
ClinVar RCV Id: RCV002297142
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly673Ala
CA346729097
NM_000251.3:c.2018G>C