Canonical Allele Identifier: PA2741904131
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2997666
ClinVar RCV Id: RCV003854265 RCV004369490
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ile283Thr
CA356737002
NM_003924.4:c.848T>C