Canonical Allele Identifier: PA263769
Gene: SLC7A7 HGNC NCBI

Linked Data

ClinVar Variation Id: 56349
ClinVar RCV Id: RCV000049762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119578.1:p.Asn365Tyr
CA263766
NM_001126106.4:c.1093A>T