Allele Registry

Canonical Allele Identifier: PA263822

Gene: SLC7A7 HGNC NCBI

ClinVar Variation Id: 56368

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119578.1:p.Phe152Leu	CA263819 NM_001126106.4:c.454T>C CA388921982 NM_001126106.4:c.456C>A CA388921983 NM_001126106.4:c.456C>G