Canonical Allele Identifier: PA2741979209
Gene: SLC7A14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2720052
ClinVar RCV Id: RCV003546318
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066000.2:p.Val311Leu
CA355492188
NM_020949.3:c.931G>C
CA355492189
NM_020949.3:c.931G>T