Canonical Allele Identifier: PA2827426662
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_001334988.1:p.Gly368Ser
CA1890055
NM_001348059.2:c.1102G>A