Allele Registry

Canonical Allele Identifier: PA112438

Gene: KRT9 HGNC NCBI

ClinVar RCV:

RCV000003138

RCV000056453

ClinVar Variation:

3002

HGVS (amino-acid)	Matching Registered Transcripts
NP_000217.2:p.Met157Val	CA115908 NM_000226.4:c.469A>G