Canonical Allele Identifier: PA161483
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 135035
ClinVar RCV Id: RCV000459859 RCV000121808 RCV001785471 RCV002408628 RCV003474730
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gly276Ser
CA161481
NM_003924.4:c.826G>A