Canonical Allele Identifier: PA104922
Gene: KRT6C HGNC NCBI

Linked Data

ClinVar Variation Id: 126527
ClinVar RCV Id: RCV000114418 RCV000255266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775109.2:p.Glu472Lys
CA151187
NM_173086.5:c.1414G>A