Canonical Allele Identifier: PA1139676333
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 925817
ClinVar RCV Id: RCV001187986
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala50Ser
CA46667075
NM_000251.3:c.148G>T