Canonical Allele Identifier: PA645427085
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 242392
ClinVar RCV Id: RCV000674391 RCV000763276 RCV001004800 RCV001854837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg657Trp
CA16616838
NM_000260.4:c.1969C>T