Canonical Allele Identifier: PA2499261239
Gene: MSH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1002226

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002430.3:p.Met360Ile
CA3327793
NM_002439.5:c.1080G>C
CA360268017
NM_002439.5:c.1080G>A
CA360268019
NM_002439.5:c.1080G>T