Allele Registry

Canonical Allele Identifier: PA2829372287

Gene: KRT13 HGNC NCBI

ClinVar RCV:

RCV001731064

ClinVar Variation:

1300083

HGVS (amino-acid)	Matching Registered Transcripts
NP_002265.3:p.Thr298Ala	CA8560617 NM_002274.4:c.892A>G