Canonical Allele Identifier: PA1139751876
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 917961
ClinVar RCV Id: RCV001175228
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714915.3:p.Val136Leu
CA371685957
NM_153704.6:c.406G>C
CA371685958
NM_153704.6:c.406G>T