Canonical Allele Identifier: PA2499230115
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1171566
ClinVar RCV Id: RCV001524763
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Phe826Leu
CA346730583
NM_000251.3:c.2476T>C
CA346730593
NM_000251.3:c.2478T>A
CA346730595
NM_000251.3:c.2478T>G