Canonical Allele Identifier: PA2573166147
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1513483

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Phe46Leu
CA028303
NM_000257.4:c.138T>A
CA389053776
NM_000257.4:c.138T>G
CA389053784
NM_000257.4:c.136T>C