Canonical Allele Identifier: PA916003922
Gene: CORO7-PAM16 HGNC NCBI

Linked Data

ClinVar Variation Id: 585054
ClinVar RCV Id: RCV000709807 RCV002532893
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001188408.1:p.Arg961Gly
CA394603500
NM_001201479.2:c.2881C>G