Canonical Allele Identifier: PA2825613171
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 939433

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Tyr1505His
CA4475365
NM_001127487.2:c.4513T>C