Canonical Allele Identifier: PA287446
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 127642
ClinVar RCV Id: RCV000115526 RCV000475276 RCV000567258 RCV001269195 RCV003467047 RCV003997277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys110Gln
CA021018
NM_000251.3:c.328A>C