Canonical Allele Identifier: PA217358
Gene: KRT6A HGNC NCBI

Linked Data

ClinVar Variation Id: 14634

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005545.1:p.Asn172del
CA217357
NM_005554.4:c.516_518del