Canonical Allele Identifier: PA130594
Gene: TMEM231 HGNC NCBI

Linked Data

ClinVar Variation Id: 39822
ClinVar RCV Id: RCV000033042 RCV000255979 RCV000543480 RCV003155046 RCV002513311
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070884.2:p.Asp262Asn
CA130593
NM_001077416.2:c.784G>A