Canonical Allele Identifier: PA645498292
Gene: SLC27A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 285420
ClinVar RCV Id: RCV000380668 RCV000954520 RCV003940009
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036386.1:p.Met539Thr
CA9717905
NM_012254.3:c.1616T>C