Canonical Allele Identifier: PA2826464812
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 218040
ClinVar RCV Id: RCV000201977 RCV000205853 RCV000491320 RCV000656880 RCV003226247 RCV003462356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Arg555Leu
CA210371
NM_001258281.1:c.1664G>T