Canonical Allele Identifier: PA174519
Gene: KRT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 161644
ClinVar RCV Id: RCV000149180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006112.3:p.Asp253Tyr
CA174518
NM_006121.4:c.757G>T