Canonical Allele Identifier: PA299391
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182595
ClinVar RCV Id: RCV000160635 RCV000588459 RCV000409531 RCV001255213 RCV001084278 RCV004528902 RCV003492654 RCV003323295
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Phe19Leu
CA021396
NM_000251.3:c.55T>C
CA346728595
NM_000251.3:c.57C>A
CA346728597
NM_000251.3:c.57C>G