Canonical Allele Identifier: PA105652
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102716
ClinVar RCV Id: RCV000088964 RCV000560269
ClinVar Variation Id: 1384858
ClinVar RCV Id: RCV001897836
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly171Arg
CA229598
NM_000277.3:c.511G>A
CA386297069
NM_000277.3:c.511G>C