Allele Registry

Canonical Allele Identifier: PA105870

Gene: KRT17 HGNC NCBI

ClinVar Allele:

29637

ClinVar RCV:

RCV000015702

RCV000056523

ClinVar Variation:

14598

HGVS (amino-acid)	Matching Registered Transcripts
NP_000413.1:p.Leu99Pro	CA216623 NM_000422.3:c.296T>C