Canonical Allele Identifier: PA2825109740
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1755743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val411Phe
CA389051073
NM_000257.4:c.1231G>T