Canonical Allele Identifier: PA112316
Gene: KRT9 HGNC NCBI

Linked Data

ClinVar Variation Id: 3000
ClinVar RCV Id: RCV000003136 RCV000056463
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000217.2:p.Asn161Lys
CA115906
NM_000226.4:c.483T>A
CA399500939
NM_000226.4:c.483T>G