Canonical Allele Identifier: PA2826464766
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1471356
ClinVar RCV Id: RCV002002627 RCV004011021 RCV004042166
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.His544Arg
CA346728369
NM_001258281.1:c.1631A>G