Canonical Allele Identifier: PA2828320427
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43196

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Glu957Asp
CA278647
NM_001369365.1:c.2871G>T
CA381943396
NM_001369365.1:c.2871G>C