Canonical Allele Identifier: PA645427050
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 306170
ClinVar RCV Id: RCV000259771 RCV000299486 RCV000354619 RCV000825399 RCV001056085 RCV001276679
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Ala601Thr
CA6197616
NM_000260.4:c.1801G>A