Allele Registry

Canonical Allele Identifier: PA112463

Gene: KRT9 HGNC NCBI

ClinVar RCV:

RCV000003143

RCV000056471

ClinVar Variation:

3007

HGVS (amino-acid)	Matching Registered Transcripts
NP_000217.2:p.Val171Met	CA115913 NM_000226.4:c.511G>A