Canonical Allele Identifier: PA2829202016
Gene: TOMT HGNC NCBI

Linked Data

ClinVar Variation Id: 305997
ClinVar RCV Id: RCV000386764
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380429.1:p.Pro165Ser
CA10640066
NM_001393500.2:c.493C>T