Canonical Allele Identifier: PA1139713170
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 952233
ClinVar RCV Id: RCV001224299 RCV002418779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gly270Glu
CA356737100
NM_003924.4:c.809G>A