ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2829372266
Gene: KRT13
HGNC
NCBI
Linked Data
ClinVar Variation Id:
323095
ClinVar RCV Id:
RCV000342351
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_002265.3:p.Val204Met
CA8560707
NM_002274.4:c.610G>A