Canonical Allele Identifier: PA101601
Gene: SLC7A7 HGNC NCBI
ClinVar RCV:
RCV000049758
ClinVar Variation:
56345
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119577.1:p.Ser53Leu
CA263752
NM_001126105.3:c.158C>T