Canonical Allele Identifier: PA2579910014
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2819811
ClinVar RCV Id: RCV003760980
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val78Leu
CA346729489
NM_000251.3:c.232G>C