Canonical Allele Identifier: PA2825112140
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3074308
ClinVar RCV Id: RCV004012850

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val1017Ile
CA389045779
NM_000257.4:c.3049G>A