Canonical Allele Identifier: PA2580147551
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2141298
ClinVar RCV Id: RCV003056887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Met130Leu
CA381931446
NM_001127180.2:c.388A>C
CA381931448
NM_001127180.2:c.388A>T