Canonical Allele Identifier: PA2825455796
Gene: SLC29A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 429191
ClinVar RCV Id: RCV000492821
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001071645.1:p.Thr387Pro
CA364311409
NM_001078177.2:c.1159A>C