Canonical Allele Identifier: PA2573231133
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1524671
ClinVar RCV Id: RCV002031890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gly237Ala
CA356737310
NM_003924.4:c.710G>C