Canonical Allele Identifier: PA2741921702
Gene: KRT6B HGNC NCBI

Linked Data

ClinVar Variation Id: 2590968
ClinVar RCV Id: RCV003365960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005546.2:p.Glu162Lys
CA6580826
NM_005555.4:c.484G>A