Canonical Allele Identifier: PA2828319983
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2129348
ClinVar RCV Id: RCV003040495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Phe603Leu
CA381938332
NM_001369365.1:c.1807T>C
CA381938343
NM_001369365.1:c.1809C>A
CA381938346
NM_001369365.1:c.1809C>G