Canonical Allele Identifier: PA217367
Gene: KRT6B HGNC NCBI

Linked Data

ClinVar Variation Id: 66599
ClinVar RCV Id: RCV000057022 RCV002483085
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005546.2:p.Glu461Lys
CA217366
NM_005555.4:c.1381G>A