Canonical Allele Identifier: PA2825114550
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2141298
ClinVar RCV Id: RCV003056887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Met130Leu
CA381931446
NM_000260.4:c.388A>C
CA381931448
NM_000260.4:c.388A>T