Canonical Allele Identifier: PA915980911
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 517510
ClinVar RCV Id: RCV001276683 RCV001228041
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Met662Leu
CA6197657
NM_001127180.2:c.1984A>T
CA381939227
NM_001127180.2:c.1984A>C