Canonical Allele Identifier: PA2579917567
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1775501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg524Gly
CA346727825
NM_000251.3:c.1570C>G