Canonical Allele Identifier: PA124155
Gene: KRT17 HGNC NCBI

Linked Data

ClinVar Variation Id: 14590
ClinVar RCV Id: RCV000056515 RCV000015692 RCV000114414 RCV002496374
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000413.1:p.Arg94His
CA124154
NM_000422.3:c.281G>A