Canonical Allele Identifier: PA2825842968
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 2929937
ClinVar RCV Id: RCV003787295
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135773.1:p.His5Tyr
CA371685909
NM_001142301.1:c.13C>T