Canonical Allele Identifier: PA2741835073
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2731544
ClinVar RCV Id: RCV003580039

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Met622Leu
CA6197629
NM_001127180.2:c.1864A>T
CA381938436
NM_001127180.2:c.1864A>C