Canonical Allele Identifier: PA105911
Gene: KRT17 HGNC NCBI

Linked Data

ClinVar Variation Id: 14599
ClinVar RCV Id: RCV000015703 RCV000056524
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000413.1:p.Val102Met
CA216624
NM_000422.3:c.304G>A