Canonical Allele Identifier: PA2499230383
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1005860

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val440Ala
CA389050869
NM_000257.4:c.1319T>C