Canonical Allele Identifier: PA104113
Gene: KRT16 HGNC NCBI

Linked Data

ClinVar Variation Id: 14604

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005548.2:p.Arg127Pro
CA217385
NM_005557.4:c.380G>C