Allele Registry

Canonical Allele Identifier: PA112077

Gene: KRT12 HGNC NCBI

ClinVar RCV:

RCV000008385

RCV000056420

ClinVar Variation:

7923

HGVS (amino-acid)	Matching Registered Transcripts
NP_000214.1:p.Arg135Gly	CA119159 NM_000223.4:c.403A>G