Allele Registry

Canonical Allele Identifier: PA2741816402

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV003694156

ClinVar Variation:

2830246

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Arg416Ser	CA8562467 NM_000526.5:c.1246C>A