Canonical Allele Identifier: PA645426520
Gene: SLC7A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 328743
ClinVar RCV Id: RCV000396840 RCV000884355
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055085.1:p.Pro468Leu
CA9358395
NM_014270.5:c.1403C>T