Canonical Allele Identifier: PA299309
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182558
ClinVar RCV Id: RCV000160583 RCV000198641 RCV000492025 RCV000662679 RCV002265636 RCV003998470
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asp461Ala
CA018117
NM_000251.3:c.1382A>C