Allele Registry

Canonical Allele Identifier: PA645294275

Gene: KRT16 HGNC NCBI

ClinVar RCV:

RCV000478068

ClinVar Variation:

419351

HGVS (amino-acid)	Matching Registered Transcripts
NP_005548.2:p.Met121Arg	CA16620406 NM_005557.4:c.362T>G