Canonical Allele Identifier: PA2580299350
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2131964
ClinVar RCV Id: RCV003055915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ala265Gly
CA356737126
NM_003924.4:c.794C>G