Allele Registry

Canonical Allele Identifier: PA916055524

Gene: KRT13 HGNC NCBI

ClinVar Variation Id: 323101

HGVS (amino-acid)	Matching Registered Transcripts
NP_705694.3:p.Ala146Gly	CA8560795 NM_153490.3:c.437C>G