Canonical Allele Identifier: PA2499287310
Gene: SLC7A14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1046264
ClinVar RCV Id: RCV001350803 RCV003888056 RCV004036638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066000.2:p.Thr318Met
CA2701755
NM_020949.3:c.953C>T