Canonical Allele Identifier: PA2579921066
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2993411
ClinVar RCV Id: RCV003850506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile735Leu
CA346729426
NM_000251.3:c.2203A>C