Canonical Allele Identifier: PA2825116306
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 881262
ClinVar RCV Id: RCV001110162 RCV001110923 RCV001110161
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Asp1030Glu
CA381944308
NM_000260.4:c.3090C>A
CA381944310
NM_000260.4:c.3090C>G