Canonical Allele Identifier: PA2573221872
Gene: MSH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1475289
ClinVar RCV Id: RCV001976125

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002430.3:p.Asp343Glu
CA360267814
NM_002439.5:c.1029T>A
CA360267815
NM_002439.5:c.1029T>G