Canonical Allele Identifier: PA2580439898
Gene: SLC7A14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2041749
ClinVar RCV Id: RCV002903213
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066000.2:p.Glu319Lys
CA2701752
NM_020949.3:c.955G>A