Canonical Allele Identifier: PA105803
Gene: KRT17 HGNC NCBI

Linked Data

ClinVar Variation Id: 14589
ClinVar RCV Id: RCV000015691 RCV000056509
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000413.1:p.Asn92His
CA124153
NM_000422.3:c.274A>C