Canonical Allele Identifier: PA2579923691
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2852498
ClinVar RCV Id: RCV003758648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys890Asn
CA346731480
NM_000251.3:c.2670G>T
CA346731481
NM_000251.3:c.2670G>C