Canonical Allele Identifier: PA915976394
Gene: SLC16A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 806191
ClinVar RCV Id: RCV000994074
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003042.3:p.Ser315Thr
CA341827866
NM_003051.4:c.943T>A