Canonical Allele Identifier: PA2829456297
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 413924
ClinVar RCV Id: RCV000463585
ClinVar Variation Id: 467740
ClinVar RCV Id: RCV000560548
ClinVar Variation Id: 699464
ClinVar RCV Id: RCV000867295

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ala252_Ala260del
CA2901427
NM_003924.4:c.747_773del
CA2901439
NM_003924.4:c.735_761del
CA2901443
NM_003924.4:c.729_755del
CA551141165
NM_003924.4:c.741_767del