Canonical Allele Identifier: PA2741921753
Gene: KRT16 HGNC NCBI

Linked Data

ClinVar Variation Id: 2519518
ClinVar RCV Id: RCV003270203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005548.2:p.Arg150Cys
CA8563268
NM_005557.4:c.448C>T