Canonical Allele Identifier: PA338685
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 216353
ClinVar RCV Id: RCV000199509 RCV000215183 RCV000411596
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala765Thr
CA338683
NM_000251.3:c.2293G>A