Canonical Allele Identifier: PA2825450112
Gene: TMEM231 HGNC NCBI

Linked Data

ClinVar Variation Id: 2118927
ClinVar RCV Id: RCV003054401
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070886.1:p.Pro164Ala
CA396806780
NM_001077418.3:c.490C>G