Canonical Allele Identifier: PA658673070
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455567
ClinVar RCV Id: RCV000534450 RCV001805149
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro837Ser
CA346730711
NM_000251.3:c.2509C>T