Canonical Allele Identifier: PA2828735957
Gene: CCDC78 HGNC NCBI

Linked Data

ClinVar Variation Id: 473257
ClinVar RCV Id: RCV000534408 RCV001755887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364959.1:p.Pro122Leu
CA7789638
NM_001378030.1:c.365C>T