Canonical Allele Identifier: PA106008
Gene: KRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 9310
ClinVar RCV Id: RCV000009895 RCV000009894 RCV000056532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000414.2:p.Glu487Lys
CA120291
NM_000423.3:c.1459G>A