Canonical Allele Identifier: PA2573217649
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1411232

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Pro660Leu
CA4474542
NM_001458.5:c.1979C>T