Canonical Allele Identifier: PA2573170947
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1499780
ClinVar RCV Id: RCV002042420

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000517.3:p.Ser55Pro
CA399483236
NM_000526.5:c.163T>C