Canonical Allele Identifier: PA915980659
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 291005
ClinVar RCV Id: RCV000726586 RCV001109571 RCV001109572 RCV001109573
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Ala226Thr
CA6197213
NM_001127180.2:c.676G>A