Canonical Allele Identifier: PA916037723
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102910
ClinVar RCV Id: RCV000089174 RCV000666332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Lys320Asn
CA229871
NM_001354304.2:c.960G>C
CA386291550
NM_001354304.2:c.960G>T