Canonical Allele Identifier: PA2829328931
Gene: FLNA HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Ala2547Val
CA415180181
NM_001456.4:c.7640C>T