Canonical Allele Identifier: PA263859
Gene: SLC7A7 HGNC NCBI

Linked Data

ClinVar Variation Id: 56383
ClinVar RCV Id: RCV000049796

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119578.1:p.Arg333Met
CA263856
NM_001126106.4:c.998G>T