Canonical Allele Identifier: PA106270
Gene: SLC7A14 HGNC NCBI

Linked Data

ClinVar Variation Id: 126447
ClinVar RCV Id: RCV000114375
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066000.2:p.Phe708Val
CA151151
NM_020949.3:c.2122T>G