Allele Registry

Canonical Allele Identifier: PA915958940

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV000487370

ClinVar Variation:

419836

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Arg388His	CA8562484 NM_000526.5:c.1163G>A