Canonical Allele Identifier: PA915965634
Gene: KRT17 HGNC NCBI

Linked Data

ClinVar Variation Id: 808261
ClinVar RCV Id: RCV000996533
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000413.1:p.Pro127Ser
CA8563777
NM_000422.3:c.379C>T