Allele Registry

Canonical Allele Identifier: PA112194

Gene: KRT12 HGNC NCBI

ClinVar RCV:

RCV000008387

RCV000056412

ClinVar Variation:

7925

HGVS (amino-acid)	Matching Registered Transcripts
NP_000214.1:p.Tyr429Asp	CA119161 NM_000223.4:c.1285T>G