Canonical Allele Identifier: PA101521
Gene: SLC7A7 HGNC NCBI

Linked Data

ClinVar Variation Id: 56378
ClinVar RCV Id: RCV000049791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119577.1:p.Leu261Pro
CA263848
NM_001126105.3:c.782T>C