Allele Registry

Canonical Allele Identifier: PA112297

Gene: KRT9 HGNC NCBI

ClinVar RCV:

RCV000056459

ClinVar Variation:

66154

HGVS (amino-acid)	Matching Registered Transcripts
NP_000217.2:p.Asn161His	CA216559 NM_000226.4:c.481A>C