Canonical Allele Identifier: PA645455288
Gene: DIP2B HGNC NCBI

Linked Data

ClinVar Variation Id: 376904
ClinVar RCV Id: RCV000425066
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775873.2:p.Cys333Ser
CA16603207
NM_173602.3:c.998G>C
CA384836418
NM_173602.3:c.997T>A