Canonical Allele Identifier: PA2499260191
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1237029
ClinVar RCV Id: RCV001639544

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Arg3530Ser
CA1103268
NM_002016.2:c.10590G>T
CA342068649
NM_002016.2:c.10590G>C