Canonical Allele Identifier: PA658664458
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 467748
ClinVar RCV Id: RCV000547484 RCV001027018 RCV003129903
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ala266Ser
CA356737122
NM_003924.4:c.796G>T