Canonical Allele Identifier: PA2580127379
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1972666
ClinVar RCV Id: RCV002730685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000517.3:p.Arg30Leu
CA399483601
NM_000526.5:c.89G>T