Canonical Allele Identifier: PA2741904114
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2625344
ClinVar RCV Id: RCV003380103

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Pro269Arg
CA356737106
NM_003924.4:c.806C>G