Canonical Allele Identifier: PA102604
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 212409
ClinVar RCV Id: RCV000192720 RCV000201747 RCV003765239
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714915.3:p.Lys99Asn
CA205731
NM_153704.6:c.297G>T
CA371685679
NM_153704.6:c.297G>C