Canonical Allele Identifier: PA263774
Gene: SLC7A7 HGNC NCBI

Linked Data

ClinVar Variation Id: 56351
ClinVar RCV Id: RCV000049764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119578.1:p.Ser386Arg
CA263771
NM_001126106.4:c.1158C>A
CA388922496
NM_001126106.4:c.1158C>G
CA388922506
NM_001126106.4:c.1156A>C