Canonical Allele Identifier: PA2580527776
Gene: KCTD7 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_694578.1:p.Thr75Ile
CA367695594
NM_153033.5:c.224C>T