Canonical Allele Identifier: PA105792
Gene: KRT17 HGNC NCBI

Linked Data

ClinVar Variation Id: 14586
ClinVar RCV Id: RCV000015688 RCV000056510
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000413.1:p.Asn92Asp
CA216607
NM_000422.3:c.274A>G