Canonical Allele Identifier: PA2826465365
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 216352
ClinVar RCV Id: RCV000196465 RCV000560982 RCV000589091 RCV001140258 RCV002500622 RCV003997019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Thr688Ala
CA035098
NM_001258281.1:c.2062A>G