Canonical Allele Identifier: PA2579919741
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2453504
ClinVar RCV Id: RCV003182959
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val655Leu
CA346728804
NM_000251.3:c.1963G>C
CA346728805
NM_000251.3:c.1963G>T