Canonical Allele Identifier: PA2829598883
Gene: KRT6B HGNC NCBI

Linked Data

ClinVar Variation Id: 3116577
ClinVar RCV Id: RCV004414425
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005546.2:p.Leu148Phe
CA6580852
NM_005555.4:c.442C>T