Canonical Allele Identifier: PA110769
Gene: TBC1D24 HGNC NCBI

Linked Data

ClinVar Variation Id: 50
ClinVar RCV Id: RCV000000067

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186036.1:p.Phe251Leu
CA339788
NM_001199107.2:c.751T>C
CA394377158
NM_001199107.2:c.753C>A
CA394377161
NM_001199107.2:c.753C>G