Canonical Allele Identifier: PA2573306422
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 1355132
ClinVar RCV Id: RCV001866767
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714915.3:p.Lys126Gln
CA371685871
NM_153704.6:c.376A>C