Canonical Allele Identifier: PA101553
Gene: SLC7A7 HGNC NCBI
ClinVar Allele:
71002
ClinVar RCV:
RCV000049776
ClinVar Variation:
56363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119577.1:p.Met50Lys
CA263805
NM_001126105.3:c.149T>A