Canonical Allele Identifier: PA915997757
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 822408
ClinVar RCV Id: RCV001017748

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Thr281Asn
CA356737027
NM_003924.4:c.842C>A