Canonical Allele Identifier: PA2826463087
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479819
ClinVar RCV Id: RCV000575601 RCV000723272 RCV001858105 RCV004000857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala141Ser
CA46678596
NM_001258281.1:c.421G>T