Canonical Allele Identifier: PA658808735
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 539418
ClinVar RCV Id: RCV000649152 RCV003153789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Asp645Ala
CA369227397
NM_001458.5:c.1934A>C