Canonical Allele Identifier: PA2825112703
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3072281
ClinVar RCV Id: RCV004012311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val1430Leu
CA389040213
NM_000257.4:c.4288G>T
CA389040216
NM_000257.4:c.4288G>C