Allele Registry

Canonical Allele Identifier: PA104172

Gene: KRT16 HGNC NCBI

ClinVar RCV:

RCV000015710

RCV000057034

ClinVar Variation:

14606

HGVS (amino-acid)	Matching Registered Transcripts
NP_005548.2:p.Leu124Arg	CA217381 NM_005557.4:c.371T>G