Canonical Allele Identifier: PA2826704214
Gene: SLC28A1 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274690.1:p.Val189Ile
CA7710450
NM_001287761.2:c.565G>A