Canonical Allele Identifier: PA915984839
Gene: SLC14A1 HGNC NCBI
ClinVar RCV:
RCV000019293
ClinVar Variation:
17720
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139509.1:p.Ser347Pro
CA127342
NM_001146037.1:c.1039T>C