Canonical Allele Identifier: PA2826465431
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 220156
ClinVar RCV Id: RCV000206397 RCV000219799 RCV000759827
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile704Thr
CA035315
NM_001258281.1:c.2111T>C