Canonical Allele Identifier: PA2826464514
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90724
ClinVar RCV Id: RCV000076221 RCV000491785 RCV001357409 RCV003452847 RCV003593896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ser488Thr
CA018877
NM_001258281.1:c.1463G>C