Canonical Allele Identifier: PA101477
Gene: SLC7A7 HGNC NCBI

Linked Data

ClinVar Variation Id: 56349
ClinVar RCV Id: RCV000049762
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119577.1:p.Asn365Tyr
CA263766
NM_001126105.3:c.1093A>T