Canonical Allele Identifier: PA658805648
Gene: SLC27A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 499339
ClinVar RCV Id: RCV000597621
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036386.1:p.Val637Leu
CA407946394
NM_012254.3:c.1909G>C