Canonical Allele Identifier: PA112365
Gene: KRT9 HGNC NCBI

Linked Data

ClinVar Variation Id: 3008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000217.2:p.Leu160Phe
CA115914
NM_000226.4:c.478C>T