Canonical Allele Identifier: PA2499265172
Gene: PHOX2B HGNC NCBI

Linked Data

ClinVar Variation Id: 997541
ClinVar RCV Id: RCV001292764 RCV003517322
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003915.2:p.Ala53Ser
CA356740956
NM_003924.4:c.157G>T