Canonical Allele Identifier: PA104092
Gene: KRT6B HGNC NCBI

Linked Data

ClinVar Variation Id: 14633
ClinVar RCV Id: RCV000015739 RCV000057023
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005546.2:p.Glu472Lys
CA210845
NM_005555.4:c.1414G>A