Canonical Allele Identifier: PA2499265205
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1016897
ClinVar RCV Id: RCV001315969 RCV002412013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gly268Ser
CA356737113
NM_003924.4:c.802G>A