Canonical Allele Identifier: PA229199
Gene: KRT82 HGNC NCBI

Linked Data

ClinVar Variation Id: 100885
ClinVar RCV Id: RCV000087247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149022.3:p.Glu210Asp
CA229198
NM_033033.4:c.630G>C
CA384939108
NM_033033.4:c.630G>T