Canonical Allele Identifier: PA915966230
Gene: SLC10A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 501088

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000443.2:p.Pro142Leu
CA7042226
NM_000452.3:c.425C>T