Canonical Allele Identifier: PA645427139
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 229002
ClinVar RCV Id: RCV000756410 RCV001835732 RCV002503858
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Ala770Thr
CA6197804
NM_000260.4:c.2308G>A