Canonical Allele Identifier: PA891844706
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 579266
ClinVar RCV Id: RCV000702508 RCV003999729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu832Asp
CA036265
NM_000251.3:c.2496G>T
CA346730659
NM_000251.3:c.2496G>C