Canonical Allele Identifier: PA2826465491
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 245647
ClinVar RCV Id: RCV000456146 RCV000585967 RCV000569234 RCV001526856 RCV003469179
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Thr722Pro
CA035470
NM_001258281.1:c.2164A>C