Canonical Allele Identifier: PA1139682242
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 858581

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln879Lys
CA037172
NM_000251.3:c.2635C>A