Canonical Allele Identifier: PA357734
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 220533
ClinVar RCV Id: RCV000206649 RCV000216074 RCV001582711 RCV003462383 RCV003997643
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr375Ile
CA027026
NM_000251.3:c.1124C>T