Canonical Allele Identifier: PA105870
Gene: KRT17 HGNC NCBI

Linked Data

ClinVar Variation Id: 14598
ClinVar RCV Id: RCV000015702 RCV000056523
JSON-LD

Amino-acid Alleles

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