Canonical Allele Identifier: PA095770
Gene: SLC52A3 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Phe224Leu
CA339795
NM_033409.4:c.670T>C
CA407963344
NM_033409.4:c.672C>G
CA407963345
NM_033409.4:c.672C>A