Canonical Allele Identifier: PA658671941
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 485848
ClinVar RCV Id: RCV000572757 RCV003758838
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys275Thr
CA346732785
NM_000251.3:c.824A>C