Canonical Allele Identifier: PA2825843027
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 2186372
ClinVar RCV Id: RCV002606590
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135773.1:p.Gln191His
CA4807774
NM_001142301.1:c.573G>C
CA371687939
NM_001142301.1:c.573G>T