Canonical Allele Identifier: PA2580264669
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2299857
ClinVar RCV Id: RCV002878247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Ser2083Arg
CA1105341
NM_002016.2:c.6249C>G
CA342054922
NM_002016.2:c.6249C>A
CA342054946
NM_002016.2:c.6247A>C