Allele Registry

Canonical Allele Identifier: PA112365

Gene: KRT9 HGNC NCBI

ClinVar RCV:

RCV000056458

RCV003232984

ClinVar Variation:

3008

HGVS (amino-acid)	Matching Registered Transcripts
NP_000217.2:p.Leu160Phe	CA115914 NM_000226.4:c.478C>T