Canonical Allele Identifier: PA915966259
Gene: SLC10A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 500243
ClinVar RCV Id: RCV000595945 RCV000763872 RCV003927926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000443.2:p.Phe304Leu
CA7041997
NM_000452.3:c.910T>C
CA388605690
NM_000452.3:c.912C>G
CA388605691
NM_000452.3:c.912C>A