Canonical Allele Identifier: PA2828319428
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_001356294.1:p.Met119Leu
CA381931446
NM_001369365.1:c.355A>C
CA381931448
NM_001369365.1:c.355A>T