Canonical Allele Identifier: PA106236
Gene: SLC7A14 HGNC NCBI

Linked Data

ClinVar Variation Id: 126449
ClinVar RCV Id: RCV000114377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066000.2:p.Ala132Val
CA151153
NM_020949.3:c.395C>T