Canonical Allele Identifier: PA103968
Gene: KRT6A HGNC NCBI

Linked Data

ClinVar Variation Id: 66569
ClinVar RCV Id: RCV000056989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005545.1:p.Ile462Ser
CA217332
NM_005554.4:c.1385T>G