Canonical Allele Identifier: PA101464
Gene: SLC7A7 HGNC NCBI

Linked Data

ClinVar Variation Id: 56383
ClinVar RCV Id: RCV000049796
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119577.1:p.Arg333Met
CA263856
NM_001126105.3:c.998G>T