Canonical Allele Identifier: PA1139724375
Gene: MSH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 943710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002430.3:p.Asp357Glu
CA360267978
NM_002439.5:c.1071T>A
CA360267980
NM_002439.5:c.1071T>G