Canonical Allele Identifier: PA2573168826
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 1460506
ClinVar RCV Id: RCV001963323

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Asn111Lys
CA382034170
NM_000372.5:c.333C>A
CA382034171
NM_000372.5:c.333C>G