Canonical Allele Identifier: PA2573168923
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 1353057
ClinVar RCV Id: RCV001869875

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Met252Leu
CA382035336
NM_000372.5:c.754A>C
CA382035338
NM_000372.5:c.754A>T