Canonical Allele Identifier: PA2828700468
Gene: DISP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 262130
ClinVar RCV Id: RCV000244588 RCV001706384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364157.1:p.Glu103Asp
CA1408774
NM_001377228.1:c.309G>T
CA344742572
NM_001377228.1:c.309G>C