Canonical Allele Identifier: PA891866074
Gene: KRT86 HGNC NCBI

Linked Data

ClinVar Variation Id: 7610
ClinVar RCV Id: RCV000008049 RCV000056960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307127.1:p.Glu413Asp
CA118925
NM_001320198.2:c.1239G>T
CA384919289
NM_001320198.2:c.1239G>C