Allele Registry

Canonical Allele Identifier: PA112282

Gene: KRT9 HGNC NCBI

ClinVar RCV:

RCV000003132

RCV000056465

RCV000626629

ClinVar Variation:

2997

HGVS (amino-acid)	Matching Registered Transcripts
NP_000217.2:p.Arg163Trp	CA115903 NM_000226.4:c.487C>T