Canonical Allele Identifier: PA2573242887
Gene: KRT16 HGNC NCBI

Linked Data

ClinVar Variation Id: 1600047
ClinVar RCV Id: RCV002132110 RCV003978711
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005548.2:p.Arg41Cys
CA8563349
NM_005557.4:c.121C>T