Allele Registry

Canonical Allele Identifier: PA112383

Gene: KRT9 HGNC NCBI

ClinVar RCV:

RCV000003140

RCV000056469

ClinVar Variation:

3004

HGVS (amino-acid)	Matching Registered Transcripts
NP_000217.2:p.Leu168Ser	CA115910 NM_000226.4:c.503T>C