Canonical Allele Identifier: PA2826465443
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408514
ClinVar RCV Id: RCV000473566 RCV000761089 RCV001284505 RCV001015184 RCV003315429
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile708Thr
CA16611051
NM_001258281.1:c.2123T>C