Canonical Allele Identifier: PA2826549539
Gene: TSPEAR HGNC NCBI

Linked Data

ClinVar Variation Id: 684487

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258966.1:p.Tyr491His
CA10056425
NM_001272037.2:c.1471T>C