Canonical Allele Identifier: PA1139680067
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 920493
ClinVar RCV Id: RCV001179251 RCV001875929
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro616Thr
CA346728412
NM_000251.3:c.1846C>A