17 | g.41502942T>C | CA8560617 | KRT13 | c.892A>G (p.Thr298Ala) c.*489A>G (n.*489A>G) n.728A>G
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.41502942T>A | CA399482163 | KRT13 | c.892A>T (p.Thr298Ser) c.*489A>T (n.*489A>T) n.728A>T
| dbSNP gnomAD v3 gnomAD v4 |