ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA106058
Gene: KRT2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
66191
ClinVar RCV Id:
RCV000056531
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000414.2:p.Leu484Pro
CA216631
NM_000423.3:c.1451T>C