Canonical Allele Identifier: PA104104
Gene: KRT16 HGNC NCBI

Linked Data

ClinVar Variation Id: 14601
ClinVar RCV Id: RCV000015705 RCV000057038 RCV000578284 RCV002496375 RCV003415709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005548.2:p.Arg127Cys
CA124157
NM_005557.4:c.379C>T