Canonical Allele Identifier: PA105661
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102773
ClinVar RCV Id: RCV000089023 RCV000705590 RCV003390791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly218Val
CA229676
NM_000277.3:c.653G>T