Canonical Allele Identifier: PA2826464859
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 219446
ClinVar RCV Id: RCV000206123 RCV000519579 RCV000562458 RCV001201177 RCV003997560
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile567Thr
CA350189
NM_001258281.1:c.1700T>C