Canonical Allele Identifier: PA915966657
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 827451
ClinVar RCV Id: RCV001027174 RCV001066735 RCV003455140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu270Pro
CA346732763
NM_000251.3:c.809T>C