Canonical Allele Identifier: PA1139677845
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 864297
ClinVar RCV Id: RCV001071448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val307Leu
CA346732979
NM_000251.3:c.919G>C