Canonical Allele Identifier: PA103913
Gene: KRT6A HGNC NCBI

Linked Data

ClinVar Variation Id: 66586

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005545.1:p.Asn171Tyr
CA217352
NM_005554.4:c.511A>T