Canonical Allele Identifier: PA2573168813
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 1482569
ClinVar RCV Id: RCV001995697
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Asn94Lys
CA6221078
NM_000372.5:c.282C>A
CA382034057
NM_000372.5:c.282C>G