Canonical Allele Identifier: PA2825625406
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 196240
ClinVar RCV Id: RCV000177023 RCV001278603
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Asp13Glu
CA243131
NM_001127180.2:c.39C>A
CA381947551
NM_001127180.2:c.39C>G