Canonical Allele Identifier: PA2826463983
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 232572
ClinVar RCV Id: RCV000216853 RCV001072003 RCV001800565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val351Gly
CA10577969
NM_001258281.1:c.1052T>G