Allele Registry

Canonical Allele Identifier: PA112419

Gene: KRT9 HGNC NCBI

ClinVar RCV:

RCV000056454

ClinVar Variation:

66152

HGVS (amino-acid)	Matching Registered Transcripts
NP_000217.2:p.Met157Lys	CA216557 NM_000226.4:c.470T>A