Canonical Allele Identifier: PA2826463031
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182598
ClinVar RCV Id: RCV000160638 RCV000212589 RCV000556928 RCV001356798
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile128Thr
CA021473
NM_001258281.1:c.383T>C