Canonical Allele Identifier: PA645427098
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 306171
ClinVar RCV Id: RCV000295997 RCV000344917 RCV000380863 RCV001048255 RCV001526683 RCV001833447
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg686His
CA6197677
NM_000260.4:c.2057G>A