Canonical Allele Identifier: PA658812300
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 535778
ClinVar RCV Id: RCV000643953 RCV001027133 RCV003420128
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Pro269Leu
CA356737105
NM_003924.4:c.806C>T