Canonical Allele Identifier: PA105853
Gene: KRT17 HGNC NCBI

Linked Data

ClinVar Variation Id: 14595
ClinVar RCV Id: RCV000015699 RCV000056517
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000413.1:p.Leu95Gln
CA216614
NM_000422.3:c.284T>A