Canonical Allele Identifier: PA916029781
Gene: CXCR4 HGNC NCBI

Linked Data

ClinVar Variation Id: 372600
ClinVar RCV Id: RCV000413464 RCV001057995 RCV003151052
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334985.1:p.Gly406Ser
CA1890055
NM_001348056.2:c.1216G>A