Canonical Allele Identifier: PA2828321586
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 228282
ClinVar Variation Id: 2695558
ClinVar RCV Id: RCV003542162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Lys1972Arg
CA10576905
NM_001369365.1:c.5915A>G
CA2697548854
NM_001369365.1:c.5915_5916delinsGA