Canonical Allele Identifier: PA1139681825
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 845581

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Phe836Ser
CA46707710
NM_000251.3:c.2507T>C