Canonical Allele Identifier: PA2499260148
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1050112
ClinVar RCV Id: RCV001357035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Leu2415Ile
CA342047832
NM_002016.2:c.7243C>A