Canonical Allele Identifier: PA2580332210
Gene: KRT6B HGNC NCBI

Linked Data

ClinVar Variation Id: 2467387
ClinVar RCV Id: RCV003197186
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005546.2:p.Arg164Cys
CA6580824
NM_005555.4:c.490C>T