Allele Registry

Canonical Allele Identifier: PA112337

Gene: KRT9 HGNC NCBI

ClinVar RCV:

RCV000003135

RCV000056460

ClinVar Variation:

2999

HGVS (amino-acid)	Matching Registered Transcripts
NP_000217.2:p.Asn161Tyr	CA115905 NM_000226.4:c.481A>T