Canonical Allele Identifier: PA2829456482
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 3223602
ClinVar RCV Id: RCV004511417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Pro277Arg
CA356737055
NM_003924.4:c.830C>G