Canonical Allele Identifier: PA210656
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 1371
ClinVar RCV Id: RCV000001436 RCV000001437 RCV001851544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135773.1:p.Tyr432Cys
CA210653
NM_001142301.1:c.1295A>G