Canonical Allele Identifier: PA106395
Gene: KRT5 HGNC NCBI

Linked Data

ClinVar Variation Id: 14639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000415.2:p.Leu463Pro
CA216658
NM_000424.4:c.1388T>C