Canonical Allele Identifier: PA2573164987
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1448755
ClinVar RCV Id: RCV002386809 RCV001997212
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr33Ile
CA042018
NM_000251.3:c.98C>T