Canonical Allele Identifier: PA2741888077
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3041680
ClinVar RCV Id: RCV003932032
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.His871Gln
CA1107076
NM_002016.2:c.2613C>A
CA342088183
NM_002016.2:c.2613C>G