Canonical Allele Identifier: PA2741891767
Gene: KRT81 HGNC NCBI

Linked Data

ClinVar Variation Id: 2559800
ClinVar RCV Id: RCV004323901
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002272.2:p.Ser492Thr
CA384913322
NM_002281.4:c.1474T>A