Canonical Allele Identifier: PA2573062070
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1327794
ClinVar Variation Id: 2721134
ClinVar RCV Id: RCV003587056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val1674Leu
CA389037123
NM_000257.4:c.5020G>C
CA389037124
NM_000257.4:c.5020G>T