Canonical Allele Identifier: PA1139739773
Gene: SLC7A14 HGNC NCBI

Linked Data

ClinVar Variation Id: 966056
ClinVar RCV Id: RCV001240644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066000.2:p.Val338Ala
CA2701745
NM_020949.3:c.1013T>C