Canonical Allele Identifier: PA2742000132
Gene: SUCNR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2600691
ClinVar RCV Id: RCV004349636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149039.2:p.Phe29Leu
CA2671636
NM_033050.6:c.87T>G
CA355018055
NM_033050.6:c.85T>C
CA355018060
NM_033050.6:c.87T>A