Canonical Allele Identifier: PA2826465191
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479813
ClinVar RCV Id: RCV000563438 RCV000629938 RCV004000854
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile642Thr
CA346729275
NM_001258281.1:c.1925T>C