Canonical Allele Identifier: PA2826462928
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 220154
ClinVar RCV Id: RCV000203760 RCV000662969 RCV000771214 RCV001569238 RCV003997617
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile103Met
CA039056
NM_001258281.1:c.309A>G