Canonical Allele Identifier: PA645413648
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 410938

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Met300Leu
CA16614038
NM_000321.3:c.898A>C
CA388159964
NM_000321.3:c.898A>T