Canonical Allele Identifier: PA915997682
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 642737
ClinVar RCV Id: RCV000796252 RCV002360924 RCV003313148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gly231Asp
CA95828497
NM_003924.4:c.692G>A