Canonical Allele Identifier: PA345436
Gene: SLC52A2 HGNC NCBI
ClinVar Allele:
102593
ClinVar RCV:
RCV000082864
ClinVar Variation:
96702
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240745.1:p.Ala284Asp
CA345434
NM_001253816.2:c.851C>A