Canonical Allele Identifier: PA2573061947
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1324737
ClinVar RCV Id: RCV001782457
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met688Val
CA346729166
NM_000251.3:c.2062A>G