Allele Registry

Canonical Allele Identifier: PA104206

Gene: KRT16 HGNC NCBI

ClinVar RCV:

RCV000015713

RCV000057040

ClinVar Variation:

14609

HGVS (amino-acid)	Matching Registered Transcripts
NP_005548.2:p.Leu128Gln	CA217386 NM_005557.4:c.383T>A