Canonical Allele Identifier: PA112337
Gene: KRT9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2999
ClinVar RCV Id: RCV000003135 RCV000056460
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000217.2:p.Asn161Tyr
CA115905
NM_000226.4:c.481A>T