Canonical Allele Identifier: PA915954836
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 821542
ClinVar RCV Id: RCV001016051 RCV001221779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala870Val
CA346731114
NM_000251.3:c.2609C>T