Canonical Allele Identifier: PA2825112235
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2430504
ClinVar RCV Id: RCV003129060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1099Val
CA389044421
NM_000257.4:c.3296C>T