Canonical Allele Identifier: PA144502
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 56788
ClinVar RCV Id: RCV000050201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135773.1:p.Ser164Phe
CA144499
NM_001142301.1:c.491C>T