Canonical Allele Identifier: PA177389
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 164692
ClinVar RCV Id: RCV000151504 RCV000666382 RCV001073912 RCV001273494 RCV001314043
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Ala1286Thr
CA177388
NM_000260.4:c.3856G>A