Canonical Allele Identifier: PA2828036648
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2911465
ClinVar RCV Id: RCV003609785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341848.1:p.Thr145Ser
CA374115060
NM_001354919.1:c.433A>T