Allele Registry

Canonical Allele Identifier: PA916055528

Gene: KRT13 HGNC NCBI

ClinVar RCV:

RCV000395479

RCV001672536

ClinVar Variation:

323096

HGVS (amino-acid)	Matching Registered Transcripts
NP_705694.3:p.Ala187Val	CA8560743 NM_153490.3:c.560C>T