Canonical Allele Identifier: PA334201
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 188160
ClinVar RCV Id: RCV000213945 RCV000417652 RCV000759120 RCV001083940 RCV000986642 RCV001358277 RCV003491920
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Phe23Leu
CA021742
NM_000251.3:c.67T>C
CA346728641
NM_000251.3:c.69T>A
CA346728643
NM_000251.3:c.69T>G