Allele Registry

Canonical Allele Identifier: PA112316

Gene: KRT9 HGNC NCBI

ClinVar RCV:

RCV000003136

RCV000056463

ClinVar Variation:

3000

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