Canonical Allele Identifier: PA216714
Gene: KRT5 HGNC NCBI

Linked Data

ClinVar Variation Id: 66238
ClinVar RCV Id: RCV000056590

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000415.2:p.Val143Ala
CA216713
NM_000424.4:c.428T>C