Canonical Allele Identifier: PA2828319851
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 179865
ClinVar RCV Id: RCV000156665 RCV000664469 RCV001110523 RCV000979350 RCV001110522 RCV001110524
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Lys504Gln
CA185300
NM_001369365.1:c.1510A>C