Canonical Allele Identifier: PA2825669122
Gene: SLC14A1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122060.3:p.Ser347Pro
CA127342
NM_001128588.4:c.1039T>C