Canonical Allele Identifier: PA2828320097
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2503060
ClinVar RCV Id: RCV003389521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Gln687Arg
CA381939584
NM_001369365.1:c.2060A>G