Canonical Allele Identifier: PA105866
Gene: KRT17 HGNC NCBI

Linked Data

ClinVar Variation Id: 14596
ClinVar RCV Id: RCV000015700 RCV000056518
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000413.1:p.Leu95Pro
CA216615
NM_000422.3:c.284T>C