Canonical Allele Identifier: PA2828319848
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1313976
ClinVar RCV Id: RCV001771207

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Glu502Asp
CA381935798
NM_001369365.1:c.1506G>C
CA381935799
NM_001369365.1:c.1506G>T