Canonical Allele Identifier: PA357374
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 220492
ClinVar RCV Id: RCV000204214 RCV000565649 RCV001556775 RCV003315421 RCV003997641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg214Ile
CA039588
NM_000251.3:c.641G>T