Canonical Allele Identifier: PA103868
Gene: KRT81 HGNC NCBI

Linked Data

ClinVar Variation Id: 7502

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002272.2:p.Glu402Lys
CA118851
NM_002281.4:c.1204G>A