Allele Registry

Canonical Allele Identifier: PA104213

Gene: KRT16 HGNC NCBI

ClinVar RCV:

RCV000015704

RCV000057042

ClinVar Variation:

14600

HGVS (amino-acid)	Matching Registered Transcripts
NP_005548.2:p.Leu132Pro	CA217389 NM_005557.4:c.395T>C