Canonical Allele Identifier: PA103897
Gene: KRT83 HGNC NCBI

Linked Data

ClinVar Variation Id: 446110
ClinVar RCV Id: RCV000515129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002273.3:p.Glu418Lys
CA384920263
NM_002282.3:c.1252G>A