Canonical Allele Identifier: PA102575
Gene: SLC7A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2138268
ClinVar RCV Id: RCV003050535
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119807.1:p.Ser379Arg
CA9358488
NM_001126335.2:c.1137C>G
CA405198106
NM_001126335.2:c.1137C>A
CA405198118
NM_001126335.2:c.1135A>C