Canonical Allele Identifier: PA891852103
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 581301
ClinVar RCV Id: RCV002406644 RCV002232978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ala266Val
CA2901417
NM_003924.4:c.797C>T