Canonical Allele Identifier: PA155736
Gene: TMEM70 HGNC NCBI

Linked Data

ClinVar Variation Id: 130598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035703.1:p.Ala34Pro
CA155735
NM_001040613.3:c.100G>C