Canonical Allele Identifier: PA645426737
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 306153
ClinVar RCV Id: RCV000298034 RCV000355269 RCV000395630 RCV001059240 RCV001833445
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Thr54Ala
CA6197062
NM_000260.4:c.160A>G