Canonical Allele Identifier: PA915981127
Gene: FLNA HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Gly288Arg
CA121667
NM_001456.4:c.862G>A
CA415248280
NM_001456.4:c.862G>C