Canonical Allele Identifier: PA101118
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 3772
ClinVar RCV Id: RCV000003970 RCV000085939 RCV000505170 RCV000599844 RCV000623980 RCV001249700 RCV002496249 RCV003466799 RCV003387499 RCV003993735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Pro81Leu
CA227551
NM_000372.5:c.242C>T