Canonical Allele Identifier: PA645452568
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 287192
ClinVar RCV Id: RCV000344452 RCV001501683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714915.3:p.Ala36Val
CA4807516
NM_153704.6:c.107C>T