Canonical Allele Identifier: PA2579921684
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2676714
ClinVar RCV Id: RCV003470216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala771Glu
CA346729880
NM_000251.3:c.2312C>A