Canonical Allele Identifier: PA2830334176
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 2630676
ClinVar RCV Id: RCV004539031
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714915.3:p.His128Gln
CA371685894
NM_153704.6:c.384C>A
CA371685895
NM_153704.6:c.384C>G