Allele Registry

Canonical Allele Identifier: PA112087

Gene: KRT12 HGNC NCBI

ClinVar RCV:

RCV000008386

RCV000056422

ClinVar Variation:

7924

HGVS (amino-acid)	Matching Registered Transcripts
NP_000214.1:p.Arg135Ile	CA119160 NM_000223.4:c.404G>T