Allele Registry

Canonical Allele Identifier: PA112410

Gene: KRT9 HGNC NCBI

ClinVar RCV:

RCV000056456

ClinVar Variation:

66153

HGVS (amino-acid)	Matching Registered Transcripts
NP_000217.2:p.Met157Arg	CA216558 NM_000226.4:c.470T>G