Canonical Allele Identifier: PA916061888
Gene: TMEM38B HGNC NCBI

Linked Data

ClinVar Variation Id: 708103
ClinVar RCV Id: RCV000879300 RCV002536814 RCV003653417 RCV003940375
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060582.1:p.Val267Ile
CA5171016
NM_018112.3:c.799G>A