Canonical Allele Identifier: PA2741904123
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 3021927
ClinVar RCV Id: RCV003880510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Gly272Ala
CA356737087
NM_003924.4:c.815G>C