Canonical Allele Identifier: PA658671345
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455500
ClinVar RCV Id: RCV000546654 RCV000579789 RCV002274057 RCV004003736
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro5Arg
CA346728432
NM_000251.3:c.14C>G