Canonical Allele Identifier: PA2829372209
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3067411
ClinVar RCV Id: RCV003993100
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Gly1901Val
CA1105637
NM_002016.2:c.5702G>T