Canonical Allele Identifier: PA106222
Gene: KRT5 HGNC NCBI

Linked Data

ClinVar Variation Id: 66293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000415.2:p.Asp328Val
CA216806
NM_000424.4:c.983A>T