Canonical Allele Identifier: PA151012
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 126306
ClinVar RCV Id: RCV000114249 RCV002514565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135773.1:p.Gly169Arg
CA151009
NM_001142301.1:c.505G>A
CA371687759
NM_001142301.1:c.505G>C