Canonical Allele Identifier: PA106510
Gene: KRT5 HGNC NCBI

Linked Data

ClinVar Variation Id: 66212
ClinVar RCV Id: RCV000056558

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000415.2:p.Thr469Pro
CA216666
NM_000424.4:c.1405A>C