Canonical Allele Identifier: PA2579909175
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2119255
ClinVar RCV Id: RCV003032999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met26Lys
CA346728667
NM_000251.3:c.77T>A