Canonical Allele Identifier: PA106247
Gene: SLC7A14 HGNC NCBI

Linked Data

ClinVar Variation Id: 126448
ClinVar RCV Id: RCV000114376 RCV000902663 RCV003888509 RCV003925105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066000.2:p.Cys464Phe
CA151152
NM_020949.3:c.1391G>T