Canonical Allele Identifier: PA2826464411
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 127631
ClinVar RCV Id: RCV000115503 RCV000463961 RCV000491225 RCV000662996 RCV001354840 RCV003997271
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys462Gln
CA018669
NM_001258281.1:c.1384A>C