Canonical Allele Identifier: PA1139700698
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 973282
ClinVar RCV Id: RCV001249713

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Ala232Val
CA415248785
NM_001456.4:c.695C>T