Canonical Allele Identifier: PA2826462807
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142613
ClinVar RCV Id: RCV000131925 RCV001052195
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val23Leu
CA020879
NM_001258281.1:c.67G>C
CA346729561
NM_001258281.1:c.67G>T