Canonical Allele Identifier: PA104049
Gene: KRT6A HGNC NCBI

Linked Data

ClinVar Variation Id: 14635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005545.1:p.Phe174Val
CA124168
NM_005554.4:c.520T>G