Allele Registry

Canonical Allele Identifier: PA105888

Gene: KRT17 HGNC NCBI

ClinVar RCV:

RCV000015696

RCV000056508

ClinVar Variation:

14592

HGVS (amino-acid)	Matching Registered Transcripts
NP_000413.1:p.Met88Thr	CA216606 NM_000422.3:c.263T>C