Canonical Allele Identifier: PA2741816379
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2715248
ClinVar RCV Id: RCV003553203

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000517.3:p.Arg6His
CA8562840
NM_000526.5:c.17G>A