Canonical Allele Identifier: PA2826465684
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 525776
ClinVar RCV Id: RCV000630060 RCV001015812 RCV003459496
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile775Thr
CA346730757
NM_001258281.1:c.2324T>C