Canonical Allele Identifier: PA105763
Gene: KRT17 HGNC NCBI

Linked Data

ClinVar Variation Id: 14591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000413.1:p.Arg94Cys
CA124156
NM_000422.3:c.280C>T