Canonical Allele Identifier: PA1139739766
Gene: SLC7A14 HGNC NCBI

Linked Data

ClinVar Variation Id: 836551
ClinVar RCV Id: RCV001037712
ClinVar Variation Id: 853441
ClinVar RCV Id: RCV001058243
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066000.2:p.Phe336Leu
CA2701748
NM_020949.3:c.1008C>G
CA87712620
NM_020949.3:c.1006T>C
CA355492019
NM_020949.3:c.1008C>A