Allele Registry

Canonical Allele Identifier: PA2829372264

Gene: KRT13 HGNC NCBI

ClinVar RCV:

RCV000395479

RCV001672536

ClinVar Variation:

323096

HGVS (amino-acid)	Matching Registered Transcripts
NP_002265.3:p.Ala187Val	CA8560743 NM_002274.4:c.560C>T