Canonical Allele Identifier: PA913196956
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 620600
ClinVar RCV Id: RCV000761030 RCV002343612 RCV003633542
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Glu186Lys
CA356738112
NM_003924.4:c.556G>A