Canonical Allele Identifier: PA915997751
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 665766
ClinVar RCV Id: RCV000824117 RCV002415948
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gln271Pro
CA356737095
NM_003924.4:c.812A>C