Canonical Allele Identifier: PA2573214458
Gene: KRT10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1634234
ClinVar RCV Id: RCV002130600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366295.1:p.Ser42Phe
CA8548355
NM_001379366.1:c.125C>T