Canonical Allele Identifier: PA645475719
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_000242.1:p.Thr788Pro
CA035470
NM_000251.3:c.2362A>C