Canonical Allele Identifier: PA105774
Gene: KRT17 HGNC NCBI

Linked Data

ClinVar Variation Id: 14594
ClinVar RCV Id: RCV000015698 RCV000056516
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000413.1:p.Arg94Pro
CA216613
NM_000422.3:c.281G>C