Canonical Allele Identifier: PA2741894685
Gene: MSH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2586086
ClinVar RCV Id: RCV003358216

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002430.3:p.Pro346Ser
CA360267847
NM_002439.5:c.1036C>T