Canonical Allele Identifier: PA2573168829
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 1368181
ClinVar RCV Id: RCV001894582

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Val119Leu
CA382034214
NM_000372.5:c.355G>T
CA382034216
NM_000372.5:c.355G>C