Canonical Allele Identifier: PA2825165531
Gene: KRT10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1965147
ClinVar RCV Id: RCV002726586

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000412.4:p.Phe67Leu
CA399396299
NM_000421.5:c.201T>G
CA399396301
NM_000421.5:c.201T>A
CA399396310
NM_000421.5:c.199T>C