Canonical Allele Identifier: PA106058
Gene: KRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 66191
ClinVar RCV Id: RCV000056531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000414.2:p.Leu484Pro
CA216631
NM_000423.3:c.1451T>C