Canonical Allele Identifier: PA2741904023
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2563103
ClinVar RCV Id: RCV003301264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gly215Arg
CA356737534
NM_003924.4:c.643G>C