Canonical Allele Identifier: PA2580269731
Gene: MSH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1779157
ClinVar RCV Id: RCV002401374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002430.3:p.Ala353Gly
CA360267930
NM_002439.5:c.1058C>G