Canonical Allele Identifier: PA216757
Gene: KRT5 HGNC NCBI

Linked Data

ClinVar Variation Id: 66262
ClinVar RCV Id: RCV000056619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000415.2:p.Ile183Thr
CA216756
NM_000424.4:c.548T>C