Canonical Allele Identifier: PA263828
Gene: SLC7A7 HGNC NCBI
ClinVar RCV:
RCV000049784
ClinVar Variation:
56371
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119578.1:p.Thr188Ile
CA263825
NM_001126106.4:c.563C>T