Canonical Allele Identifier: PA2580299357
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2089165
ClinVar RCV Id: RCV003012007 RCV003475462
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gly276_Pro277insThrGly
CA2580070994
NM_003924.4:c.828_829insACCGGC