Allele Registry

Canonical Allele Identifier: PA2826910676

Gene: FN1 HGNC NCBI

ClinVar RCV:

RCV000480973

RCV000754912

ClinVar Variation:

421465

HGVS (amino-acid)	Matching Registered Transcripts
NP_001293058.2:p.Cys231Trp	CA16617467 NM_001306129.2:c.693C>G