Allele Registry

Canonical Allele Identifier: PA112429

Gene: KRT9 HGNC NCBI

ClinVar RCV:

RCV000003142

RCV000056455

ClinVar Variation:

3006

HGVS (amino-acid)	Matching Registered Transcripts
NP_000217.2:p.Met157Thr	CA115912 NM_000226.4:c.470T>C