Allele Registry

Canonical Allele Identifier: PA2580528836

Gene: TMEM151A HGNC NCBI

ClinVar RCV:

RCV003152481

ClinVar Variation:

2443873

HGVS (amino-acid)	Matching Registered Transcripts
NP_694998.1:p.Leu253Pro	CA381396919 NM_153266.4:c.758T>C