Allele Registry

Canonical Allele Identifier: PA105763

Gene: KRT17 HGNC NCBI

ClinVar RCV:

RCV000015694

RCV000056513

RCV000114415

ClinVar Variation:

14591

HGVS (amino-acid)	Matching Registered Transcripts
NP_000413.1:p.Arg94Cys	CA124156 NM_000422.3:c.280C>T