Canonical Allele Identifier: PA1139713173
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 855775
ClinVar RCV Id: RCV003473675 RCV001061110
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Pro279Leu
CA356737042
NM_003924.4:c.836C>T