Canonical Allele Identifier: PA2828321076
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 991570
ClinVar RCV Id: RCV001279803

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Phe1548Leu
CA381950935
NM_001369365.1:c.4642T>C
CA381950939
NM_001369365.1:c.4644C>A
CA381950940
NM_001369365.1:c.4644C>G