Canonical Allele Identifier: PA2826463000
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91134
ClinVar RCV Id: RCV000076638 RCV000581973 RCV001240116 RCV001353422 RCV003466968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu121Pro
CA021405
NM_001258281.1:c.362T>C