Allele Registry

Canonical Allele Identifier: PA104162

Gene: KRT16 HGNC NCBI

ClinVar RCV:

RCV000015709

RCV000057031

ClinVar Variation:

14605

HGVS (amino-acid)	Matching Registered Transcripts
NP_005548.2:p.Gln122Pro	CA217378 NM_005557.4:c.365A>C