Canonical Allele Identifier: PA104039
Gene: KRT6A HGNC NCBI

Linked Data

ClinVar Variation Id: 66591
ClinVar RCV Id: RCV000057014 RCV000144078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005545.1:p.Phe174Ser
CA170746
NM_005554.4:c.521T>C