Canonical Allele Identifier: PA2826463328
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 428563
ClinVar RCV Id: RCV000492013 RCV000629850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala200Thr
CA346732742
NM_001258281.1:c.598G>A