Canonical Allele Identifier: PA2741921741
Gene: KRT16 HGNC NCBI

Linked Data

ClinVar Variation Id: 2614868
ClinVar RCV Id: RCV003365014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005548.2:p.Cys4Gly
CA399497551
NM_005557.4:c.10T>G