Canonical Allele Identifier: PA916059436
Gene: GNB4 HGNC NCBI

Linked Data

ClinVar Variation Id: 640868
ClinVar RCV Id: RCV000793984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067642.1:p.Phe253Leu
CA2712414
NM_021629.4:c.759T>G
CA88740389
NM_021629.4:c.757T>C
CA355469093
NM_021629.4:c.759T>A