Canonical Allele Identifier: PA916037396
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 92738
ClinVar RCV Id: RCV000078517 RCV000150091 RCV003398669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Arg68Ser
CA273113
NM_001354304.2:c.204A>T
CA386304213
NM_001354304.2:c.204A>C