Allele Registry

Canonical Allele Identifier: PA112169

Gene: KRT12 HGNC NCBI

ClinVar RCV:

RCV000008389

RCV000056417

ClinVar Variation:

7927

HGVS (amino-acid)	Matching Registered Transcripts
NP_000214.1:p.Met129Thr	CA119163 NM_000223.4:c.386T>C