Canonical Allele Identifier: PA2826464858
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 525723
ClinVar RCV Id: RCV000629955 RCV001013601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile566Val
CA346728571
NM_001258281.1:c.1696A>G