Canonical Allele Identifier: PA2573221890
Gene: MSH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1384930
ClinVar RCV Id: RCV001902705 RCV004041344
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002430.3:p.Asp352Gly
CA360267917
NM_002439.5:c.1055A>G