Canonical Allele Identifier: PA2580332250
Gene: KRT16 HGNC NCBI

Linked Data

ClinVar Variation Id: 2217833
ClinVar RCV Id: RCV002670149

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005548.2:p.Ser33Cys
CA8563355
NM_005557.4:c.98C>G