Canonical Allele Identifier: PA2741834947
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2749577
ClinVar RCV Id: RCV003568502
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Met309Leu
CA381933037
NM_001127180.2:c.925A>C
CA381933038
NM_001127180.2:c.925A>T