Canonical Allele Identifier: PA2826464241
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 480908
ClinVar RCV Id: RCV000571070
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Arg416Ser
CA346726920
NM_001258281.1:c.1248A>C
CA346726922
NM_001258281.1:c.1248A>T