Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.4860099T>ACA124434MSX1c.200T>A (p.Met67Lys)
 ClinVar dbSNP
4g.4860099T>CCA356137358MSX1c.200T>C (p.Met67Thr)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched